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Zd

FDA UDI

Class I (US FDA UDI)

by Zhende Medical Co., Ltd.

Identity

Trade Name
ZD FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Device Name
FOAM, ADH SIL W/BORDER 4"X4" 1PK ,10PK/BX , 20BX/CS FDA UDI
Description
FOAM, ADH SIL W/BORDER 4"X4" 1PK ,10PK/BX , 20BX/CS FDA UDI

Identifiers

Primary DI / UDI-DI
06926515439484 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Exudate-absorbent dressing, non-gel, non-antimicrobial

Zd by Zhende Medical Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, non-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3da50faa-a291-4de7-a552-02579b96361c 32 fields · synced May 30, 2026