← Back to catalogue

BIOER GenePure 96 Nucleic Acid Purification System

FDA UDI

Class I (US FDA UDI)

by Hangzhou Bioer Technology Co., Ltd.

Identity

Trade Name
BIOER GenePure 96 Nucleic Acid Purification System FDA UDI
Generic Name
Nucleic acid sample preparation instrument IVD FDA UDI
Device Name
For the detail information, please refer to the IFU. FDA UDI
Model / Reference
NPA-96E FDA UDI
Description
For the detail information, please refer to the IFU. FDA UDI

Identifiers

Primary DI / UDI-DI
06973843220185 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Nucleic acid sample preparation instrument 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid sample preparation instrument IVD

BIOER GenePure 96 Nucleic Acid Purification System by Hangzhou Bioer Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 103c520d-4270-471c-a2c1-c329fd9d9cdf 33 fields · synced May 31, 2026