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LiquiBand XL

FDA UDI

Class II (US FDA UDI)

by Advanced Medical Solutions (Plymouth), Ltd.

Identity

Trade Name
LiquiBand XL FDA UDI
Generic Name
Wound closure set, topical FDA UDI
Model / Reference
72014046A FDA UDI

Identifiers

Primary DI / UDI-DI
05036912001656 FDA UDI
510(k) Number
K211878 FDA UDI
FDA Product Code
OMD FDA UDI
GMDN Term
Wound closure set, topical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4011 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound closure set, topical

LiquiBand XL by Advanced Medical Solutions (Plymouth), Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound closure set, topical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b0ed2717-b32c-4592-bef6-5e2ba526e283 34 fields · synced May 30, 2026