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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
Medical bag FDA UDI
Device Name
Specimen Bag - US (perforation) 6"x9" w/absorbent pad FDA UDI
Model / Reference
AB001 FDA UDI
Description
Specimen Bag - US (perforation) 6"x9" w/absorbent pad FDA UDI

Identifiers

Primary DI / UDI-DI
06947462405315 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
Medical bag FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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: Medical bag

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 Medical bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9dd6c757-7a0a-4760-be41-b000a587991d 33 fields · synced May 31, 2026