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Liquifix Fix8

FDA UDI

Class III (US FDA UDI)

by Advanced Medical Solutions (Plymouth), Ltd.

Identity

Trade Name
LIQUIFIX FIX8 FDA UDI
Generic Name
Surgical internal adhesive/sealant, synthetic polymer FDA UDI
Device Name
LIQUIFIX FIX8, non-penetrating hernia mesh fixation, 40+ liquid anchors FDA UDI
Model / Reference
72014032 FDA UDI
Description
LIQUIFIX FIX8, non-penetrating hernia mesh fixation, 40+ liquid anchors FDA UDI

Identifiers

Primary DI / UDI-DI
05036912001410 FDA UDI
PMA Number
P220024 FDA UDI
FDA Product Code
PLJ FDA UDI
GMDN Term
Surgical internal adhesive/sealant, synthetic polymer FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Safe FDA UDI

Category: Surgical internal adhesive/sealant, synthetic polymer

Liquifix Fix8 by Advanced Medical Solutions (Plymouth), Ltd. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical internal adhesive/sealant, synthetic polymer.

Cleared under the same submission

P220024 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Medical Solutions (Plymouth), Ltd.

Sources (1)

  • FDA UDI 9b1a83cf-da59-41ce-a089-009aeaaeced4 34 fields · synced Jun 8, 2026