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Simplicity TM Dx Extraction Kit

FDA UDI

Class I (US FDA UDI)

by Hangzhou Bioer Technology Co., Ltd.

Identity

Trade Name
Simplicity TM Dx Extraction Kit FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Device Name
DNA/RNA Extraction / purification For the detail information, please refer to the IFU. FDA UDI
Model / Reference
EXT-DoR-MD32P FDA UDI
Description
DNA/RNA Extraction / purification For the detail information, please refer to the IFU. FDA UDI

Identifiers

Primary DI / UDI-DI
06973843228891 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nucleic acid extraction/isolation kit IVD

Simplicity TM Dx Extraction Kit by Hangzhou Bioer Technology 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 ea87db77-2a43-4b5e-aacd-fbd75ea15228 33 fields · synced May 30, 2026