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Simplicity TM Dx Extraction System

FDA UDI

Class I (US FDA UDI)

by Hangzhou Bioer Technology Co., Ltd.

Identity

Trade Name
Simplicity TM Dx Extraction 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
EQP-ETR-MD32 FDA UDI
Description
For the detail information, please refer to the IFU. FDA UDI

Identifiers

Primary DI / UDI-DI
06973843220819 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

Simplicity TM Dx Extraction System 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 sample preparation instrument IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a52a02a4-d6a4-4ee3-b706-61048b0f7de7 33 fields · synced May 30, 2026