← Back to catalogue

BioTeke

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref AU1001SModel AU1001,AU1001S,AU1001-96

by Bioteke Corporation (Wuxi) Co., Ltd.

Identity

Trade Name
BioTeke FDA UDI
Generic Name
Nucleic acid sample preparation instrument IVD FDA UDI
Device Name
Automated Nucleic Acid Extraction System EUDAMED
Model / Reference
AU1001S EUDAMEDFDA UDI
AU1001,AU1001S,AU1001-96 EUDAMED

Identifiers

Primary DI / UDI-DI
06974541565042 EUDAMED
06974541563666 FDA UDI
Basic UDI-DI
697454156003KX EUDAMED
FDA Product Code
JJH FDA UDI
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED
GMDN Term
Nucleic acid sample preparation instrument IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2310 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid sample preparation instrument IVD

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

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 212b16fe-0a5f-4f88-bd77-1c2f560c9da1 32 fields · synced Jul 9, 2026
  • EUDAMED 85f12c52-2d52-4012-95f2-4cc34d1dcc5f 61 fields · synced Jul 9, 2026