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LiquidSkin, 0.5g

FDA UDI

Class I (US FDA UDI)

by Chemence Medical Inc.

Identity

Trade Name
LiquidSkin, 0.5g FDA UDI
Generic Name
Skin-cover sealant FDA UDI
Model / Reference
503 5000 FDA UDI

Identifiers

Catalog Number
503 5000 FDA UDI
Primary DI / UDI-DI
00854137001740 FDA UDI
FDA Product Code
NEC FDA UDI
GMDN Term
Skin-cover sealant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 FDA UDI
Commercial Distribution
Not 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

LiquidSkin, 0.5g by Chemence Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 045587f6-0ab8-44d2-9333-f18c57edf143 35 fields · synced Sep 18, 2026