FDA UDI In Commercial Distribution 🇺🇸 United States

Merocel™

DI: 20763000616964 · Model: 440402 · MEDTRONIC XOMED, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Merocel™
Primary DI
20763000616964
Version / Model
440402
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-03-04
Public Version
1
Public Version Date
2022-03-14
Public Version Status
New
Public Device Record Key
2ea60f59-2ba4-466e-8d4d-19352564a9cf

Device Description

DRESSING 440402 MEROCEL 10PK STANDARD 8C

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 00763000616960
Primary 20763000616964

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8.0 Centimeter