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BGEcare Non-sterile Non-woven Sponge

FDA UDI

Class I (US FDA UDI)

by Henan Zhende Medical Products Co., Ltd.

Identity

Trade Name
BGEcare Non-sterile Non-woven Sponge FDA UDI
Generic Name
Non-woven gauze pad, non-sterile FDA UDI
Device Name
BGEcare Non-sterile Non-woven Sponge 2"X2", 4-Ply, 200 pieces/pack, 20 packs/carton box FDA UDI
Model / Reference
NS0602020420020NS FDA UDI
Description
BGEcare Non-sterile Non-woven Sponge 2"X2", 4-Ply, 200 pieces/pack, 20 packs/carton box FDA UDI

Identifiers

Primary DI / UDI-DI
06972403420201 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Non-woven gauze pad, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-woven gauze pad, non-sterile

BGEcare Non-sterile Non-woven Sponge by Henan Zhende Medical Products Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e2584c63-6065-459f-b135-f1987a0a9127 33 fields · synced May 31, 2026