FDA UDI In Commercial Distribution 🇺🇸 United States

MEROCEL®

DI: 20681490112509 · Model: 440406 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
MEROCEL®
Primary DI
20681490112509
Version / Model
440406
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
47d44014-6d5f-4dea-bb35-232cee36bca3

Device Description

PACKING 440406 10PK POPE 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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Unit of Use 00681490112505
Primary 20681490112509

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10.0 Centimeter