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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
Pipette tip FDA UDI
Device Name
Pipette Tip FDA UDI
Model / Reference
E1030 FDA UDI
Description
Pipette Tip FDA UDI

Identifiers

Primary DI / UDI-DI
06947462492247 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Pipette tip 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pipette tip

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 Pipette tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhejiang Gongdong Medical Technology Co., Ltd.,

Sources (1)

  • FDA UDI eff8fb04-33b0-4395-b63e-40a2b67fd84d 33 fields · synced May 30, 2026