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BioTeke

FDA UDI

Class I (US FDA UDI)

by Bioteke Corporation (Wuxi) Co., Ltd.

Identity

Trade Name
BioTeke FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Model / Reference
AU17012 FDA UDI

Identifiers

Primary DI / UDI-DI
06974541563550 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Nucleic acid extraction/isolation kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid extraction/isolation kit IVD

BioTeke by Bioteke Corporation (Wuxi) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 408dd142-8638-4e88-ac9d-bf398c130040 32 fields · synced May 30, 2026