FDA UDI In Commercial Distribution 🇺🇸 United States

MEROCEL®

DI: 20681490105266 · Model: 400421 · MEDTRONIC XOMED, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
MEROCEL®
Primary DI
20681490105266
Version / Model
400421
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2020-11-12
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
5e61c6d5-e3cc-4e0b-9c8d-5c3ca639a46d

Device Description

PACKING 400421 20PK WEIMERT EPISTAXIS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EFQ GAUZE/SPONGE, INTERNAL
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Unit of Use 00681490105262
Primary 20681490105266

Customer Contacts