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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
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI
Device Name
Non Sterile Clipped Elastic Bandage 6" x 5.5 yds FDA UDI
Model / Reference
NUMT004 FDA UDI
Description
Non Sterile Clipped Elastic Bandage 6" x 5.5 yds FDA UDI

Identifiers

Primary DI / UDI-DI
06942273317697 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Skin treatment/dressing-supportive limb/finger bandage, single-use

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

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhende Medical Co., Ltd.

Sources (1)

  • FDA UDI 6d11c513-1c17-4e63-bc34-a89a96533774 33 fields · synced Jun 1, 2026