活体切片组织能带进澳洲吗？

eqiu

请问各位足迹大神，我爸爸在国内开过刀，是左肺结节，活体切片组织，就是2片小小的玻璃，当中有些从体内取出的组织。下周来澳洲探亲，顺便想来看看这里的医生。不知道这切片会被海关没收吗？

jffh

当然，查出来还得罚款。相当于带狗狗和水果啥的。

eqiu

jffh 发表于 2015-4-16 17:01
当然，查出来还得罚款。相当于带狗狗和水果啥的。

是嘛，又听别人说放在口袋里带进来了

Sparky

为什么要带来这里看呢？这里一般的GP估计也没办法帮你看切片组织，专科的也不是想看就马上能看上，而且我觉得也不太可能说你去找个专科医生说你帮我看看这些切片有没事，然后专科医生就帮你看了啊。

ItsThere

可否把切片图像化？那样就容易传过来了。

brookrock

让国内医院病理科的把切片做成电子的，带电子图片过来给这边的病理专家看，GP一般是看不来的
或者国内的带图片的病理报告要一份带过来也行

ItsThere

切片里组织是否还有致病性。。。
不如你问问海关，我觉得未必不行。
不过你最好要知道切片资料的唯一性，偷带被没收或丢失是你的损失。

cnipac

An Import Permit is not required for human tissues, DNA, proteins, human sperm, human ova (eggs) or fluids, (excluding human antibodies and cell lines), for therapeutic use. An Import Permit is required for all other end uses.  Import Permit applications must be sent to Department of Agriculture, Canberra office for assessment, prior to importation.

This commodity is classified as a Category 2 assessment for the purposes of determining the Import Permit fee rate that applies. The fee rate is $120.00 (for any assessment period up to 1 hour) and $40.00 for each quarter hour, or part of a quarter hour, after the 1-hour period. Note that in addition to the assessment fee, an electronic lodgement fee of $125.00 or a manual lodgement fee of $225.00 also applies.

	Commodity:	Human tissues and fluids (excluding human antibodies and cell lines)
	Scientific name:	Human tissues and fluids (excluding human antibodies and cell lines)
[/td]
	Synonyms:	Show Synonyms
[/td]
		Basophil, Brain, Coagulation factor, cochlear implant, Deoxyribonucleic acid, Eosinophil, Erythrocyte, Haemoglobin, Heart, Hematocrit, Human albumin, Human blood cells, Human bodies for display, Human bodies for in vitro use, Human breast milk, Human cartilage, Human colostrum, Human DNA, Human embryos, Human enzymes, Human expressed milk, Human faeces, Human fluids, Human genetic material, Human hair, Human hormones, Human ligament, Human lymphatic fluid, Human milk, Human mRNA, mDNA, cDNA, cRNA, Human oligonucleotides, Human placenta, Human plasma, Human platelet, Human proteins, Human red cells, Human retina, Human RNA, Human saliva, Human semen, Human sera, Human serum, Human sperm, Human spleen, Human stem cells, Human sweat, Human tissues and fluids (excluding human antibodies and cell lines), Human urine, Human white cells, IVF, Kidney, Leucocyte, Liver, Lung, Lymphocyte, Monocyte, Muscle, Neutrophil, Organs, Pancreas, Placenta, Plastinated Human Bodies, Reticulocyte, Teeth, Tissue samples, Tissues samples embedded in paraffin wax, Transplant
[/td]
	Country:	All countries
	End use:	Therapeutic
	Date printed:	Apr 17 2015

The information here covers Department of Agriculture quarantine requirements only and is current on the date of transmission but may change without notice.  Department of Agriculture makes no warranties or representations with respect to the accuracy or completeness of that information and will bear no liability with  respect to that information. Importers must satisfy quarantine concerns and comply with quarantine conditions applicable at the time of entry.  The Commonwealth through Department of Agriculture is not liable for any costs arising from or associated with decisions of importers to import based on conditions  presented here which are not current at the time of importation.  It is the importer’s responsibility to verify the accuracy and completeness of the  information at the time of importation. It is the importer’s responsibility to identify and to ensure it has complied with, all requirements of any other regulatory and advisory bodies  prior to and after importation including the Australian Customs and Border Protection Service, Therapeutic Goods Administration, Department of Health and Ageing,  Department of Sustainability, Environment, Water, Population and Communities, Australian Pesticides and Veterinary Medicines Authority and any State agencies such as Departments  of Agriculture and Health and Environmental Protection authorities.   Importers should note that this list is not exhaustive.  Importers should also note that all foods imported into Australia must comply with the  provisions of the Imported Food Control Act 1992 , an Act which is administered by Department of Agriculture. Notification of the import must be provided to Department of Agriculture for all imported goods other than goods imported as accompanied baggage or goods imported via  the mail and not prescribed under the Customs Act 1901. Notification must be consistent with Quarantine Regulations 2000  (examples include a Quarantine Entry or a Quarantine declaration).

[/tr]

[/td]
	[size=+1]Condition  C5405                                          A quarantine entry is not required for most human tissues and fluids, apart from faeces, cell lines and DNA     Non-commercial All conditions under the Commercial section apply. Commercial 1.      An Import Permit is not required for human tissues, DNA, proteins, human sperm, human ova (eggs) or fluids, (excluding human antibodies and cell lines), for therapeutic use. An Import Permit is required for all other end uses.  Import Permit applications must be sent to Department of Agriculture, Canberra office for assessment, prior to importation. 2.      Product must be labelled ‘product of human origin’, or be accompanied by supporting documentation from the exporter or supplier (e.g. invoice or letter), to confirm the origin. 3.      A declaration from the importer or exporter must be provided at the time of importation stating that the products are for therapeutic use only as defined in the Therapeutic Goods Act 1989. Definition of Therapeutic Use Under Section 3 of the Therapeutic Goods Act 1989, therapeutic use means use in or in connection with: (a) preventing, diagnosing, curing or alleviating a disease, ailment, defect or injury in persons or animals; or (b) influencing, inhibiting or modifying a physiological process in persons or animals; or (c) testing the susceptibility of persons or animals to a disease or ailment; or (d) influencing, controlling or preventing conception in persons; or (e) testing for pregnancy in persons; or (f) the replacement or modification of parts of the anatomy in persons or animals. For example: Pathology specimens for the diagnosis of diseases/ailments are considered as being used for therapeutic use and therefore do not require an import permit.   Tissue/fluid samples being imported for research purposes or in-vitro use, not connected to the diagnosis of disease in an individual, are not considered to meet this definition of therapeutic use.  As such an import permit will be required. Note: Products for veterinary therapeutic use must meet the requirements of the ICON case “Veterinary therapeutics and medicines” For information relating to human antibodies and cell lines, please refer to the ICON case ‘Human antibodies and cell lines’. Applications for products which are infected with microorganisms known or with the potential to pose a human quarantine risk will be referred to the Department of Health and Ageing for advice.  This includes, but is not restricted to, products infected with human quarantinable diseases as listed below from Table 9, Section 21 of the Quarantine Proclamation 1998. Human Quarantinable Disease Also Known As Cholera Vibriocholerae Plague Yersiniapestis Rabies Lyssavirus Severe Acute Respiratory Syndrome SARS SARS associated Coronavirus Smallpox Variola virus   Poxvirus variola Viral haemorrhagic fevers of humans Ebola haemorrhagic fever (Filoviridae) Marburg  virus (Filoviridae)   Lassa Fever (Arenaviridae)   Crimean-Congo hemorrhagic fever (Nairovirus) Yellow fever Flavivirus Highly Pathogenic Avian Influenza in Humans HPAIH, Bird Flu, H5N1
	[size=+1]Condition  C9000                                           The importer must comply with all international (eg IATA) and domestic requirements concerning the safe handling, transport and labelling of biological material The importer must comply with all international (eg IATA) and domestic requirements concerning the safe handling, transport and labelling of biological material. Safety precautions shall also be maintained during shipment and handling to prevent dissemination of pathogens.
	[size=+1]Entry Management  EM0184                                             Department of Agriculture minimum documentary requirements to support assessment of all documentation All documentation presented to the Department of Agriculture as part of the import process must meet the requirements of the Minimum Documentary Requirements Policy. These requirements include: Overarching Requirements (e.g. legible, in English,     signed, dated, linked to the consignment); Document Format Requirements (e.g. as per nationally     accepted practice and standards, or on company letterhead); and Prescribed Information Requirements (e.g. treatment     certificates must include a description of the goods/packaging treated)
	[size=+1]Entry Management  EM0185                                             Information requirements to support assessment of non-commodity concerns associated with imported cargo All documentation presented to the Department of Agriculture to assist in determining the level of quarantine risk posed by transportation pathways and packaging must meet the requirements of the Non-Commodity Information Requirements Policy. These requirements address: Container cleanliness; Packaging concerns (e.g. presence of timber or     prohibited packaging material); and Destination concerns (e.g. destined for a rural unpack     location).
	[size=+1]Import Permit Fee  IPF0003                                             Import Permit Fees (where applicable) – Category 2 This commodity is classified as a Category 2 assessment for the purposes of determining the Import Permit fee rate that applies. The fee rate is $120.00 (for any assessment period up to 1 hour) and $40.00 for each quarter hour, or part of a quarter hour, after the 1-hour period. Note that in addition to the assessment fee, an electronic lodgement fee of $125.00 or a manual lodgement fee of $225.00 also applies. An assessable item means an item identified on an Import Permit application as consisting of goods of a class imported, or to be imported, from a particular country for a particular use. Further information on department’s fees and charges can be found on the Department of Agriculture website. Import Permit issuing fees are specified in the Quarantine Service Fees Determination 2005.

eqiu

Sparky 发表于 2015-4-17 09:41
为什么要带来这里看呢？这里一般的GP估计也没办法帮你看切片组织，专科的也不是想看就马上能看上，而且我觉 ...

我向GP咨询过，她说最好把国内手术后的切片组织带来，让专科医生看

eqiu

ItsThere 发表于 2015-4-17 09:52
切片里组织是否还有致病性。。。
不如你问问海关，我觉得未必不行。
不过你最好要知道切片资料的唯一性，偷 ...

国内称腊片，不可能再致病的

eqiu

cnipac 发表于 2015-4-17 10:09
An Import Permit is not required for human tissues, DNA, proteins, human sperm, human ova (eggs) or  ...

太感谢啦！

ItsThere

eqiu 发表于 2015-4-17 23:20
国内称腊片，不可能再致病的

上学时做过蜡块，时间太久不敢确定了。