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Gongdong

FDA UDI

Class I (US FDA UDI)

by Zhejiang Gongdong Medical Technology Co., Ltd.,

Identity

Trade Name
Gongdong FDA UDI
Generic Name
Clinical specimen extraction buffer IVD FDA UDI
Device Name
Quantisal Expressor (empty filter frit) with lid and ring FDA UDI
Model / Reference
G2001 FDA UDI
Description
Quantisal Expressor (empty filter frit) with lid and ring FDA UDI

Identifiers

Primary DI / UDI-DI
06947462403687 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Clinical specimen extraction buffer IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Category: Clinical specimen extraction buffer IVD

Gongdong by Zhejiang Gongdong Medical Technology Co., Ltd., — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical specimen extraction buffer IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a53dcdeb-0244-49e7-967e-ea1a39b7d7ee 33 fields · synced May 30, 2026