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Merogel Injectable

FDA UDI

Class II (US FDA UDI)

by Anika Therapeutics, Inc.

Identity

Trade Name
Merogel Injectable FDA UDI
Generic Name
Surgical anti-adhesion material, implantable, bioabsorbable, non-medicated FDA UDI
Device Name
MEROGEL Injectable is a bioresorbable nasal dressing and sinus stent and otologic gel designed to help control bleeding and to create a physical separation of mucosal surfaces with the purpose of preventing adhesions during the post-operative healing process FDA UDI
Model / Reference
640-023 FDA UDI
Description
MEROGEL Injectable is a bioresorbable nasal dressing and sinus stent and otologic gel designed to help control bleeding and to create a physical separation of mucosal surfaces with the purpose of preventing adhesions during the post-operative healing process FDA UDI

Identifiers

Catalog Number
CFN 1518000 FDA UDI
Primary DI / UDI-DI
08033549790769 FDA UDI
FDA Product Code
NHB FDA UDI
GMDN Term
Surgical anti-adhesion material, implantable, bioabsorbable, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3620 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Merogel Injectable by Anika Therapeutics, Inc. — Class II — 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 211290da-2043-41f7-a5ab-13941590b28a 36 fields · synced Jun 9, 2026