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MEROGEL 2pk 4x4cm

FDA UDI

Class I (US FDA UDI)

by Anika Therapeutics, Inc.

Identity

Trade Name
MEROGEL 2pk 4x4cm FDA UDI
Generic Name
Intranasal splint, biodegradable FDA UDI
Device Name
Merogel is used in the nasal/sinus and the middle ear/external ear canal as a space occupying dressing and/or stent, to separate mucosal surfaces and to help control minimal bleeding following surgery, and in otologic packing, to act as an adjunct to aid in the natural healing process. FDA UDI
Model / Reference
651141 FDA UDI
Description
Merogel is used in the nasal/sinus and the middle ear/external ear canal as a space occupying dressing and/or stent, to separate mucosal surfaces and to help control minimal bleeding following surgery, and in otologic packing, to act as an adjunct to aid in the natural healing process. FDA UDI

Identifiers

Catalog Number
1517002 FDA UDI
Primary DI / UDI-DI
08033549791117 FDA UDI
FDA Product Code
EMX FDA UDI
GMDN Term
Intranasal splint, biodegradable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4100 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 2pk 4x4cm by Anika Therapeutics, 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

Manufacturer
Anika Therapeutics, Inc.

Sources (1)

  • FDA UDI 7a0842e4-bb5b-4ef6-9aab-32138b54b427 35 fields · synced Jun 9, 2026