AccessGUDID - DEVICE: Merogel Nasal Dressing/Sinus Stent &Otologic Packing 4x4cm (08033549790967)

GUDID

Device Identifier (DI) Information

Brand Name: Merogel Nasal Dressing/Sinus Stent &Otologic Packing 4x4cm
Version or Model: 651-140
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 1517000
Company Name: Anika Therapeutics, Inc.

Primary DI Number: 08033549790967
Issuing Agency: GS1
Commercial Distribution End Date: June 11, 2025
Device Count: 1
Labeler D-U-N-S® Number*: 807613393 *Terms of Use
Previous DI: 08033549790721

Device Description: Medtronic MeroGel Nasal Dressing/Sinus stent and Otologic Packing 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.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
41493	Intranasal splint, biodegradable	A bioabsorbable device intended to be placed via a nostril into the nasal cavity after surgery or trauma to help minimize bleeding by tamponade effect, prevent adhesions between the mucosal surfaces, and/or provide support to the surrounding tissues during the healing period. It is made of non-animal source material which chemically degrades after about 3 – 4 weeks and is absorbed via natural body processes, or it may be removed at the discretion of the physician. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
EMX	Balloon, Epistaxis

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: d97307cf-21e5-4f1a-a3c1-8804ca939527
Public Version Date: June 12, 2025
Public Version Number: 3
DI Record Publish Date: January 15, 2020