FDA UDI In Commercial Distribution 🇺🇸 United States

Merocel™

DI: 20763000616773 · Model: 400407 · MEDTRONIC XOMED, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Merocel™
Primary DI
20763000616773
Version / Model
400407
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2022-03-04
Public Version
2
Public Version Date
2024-11-07
Public Version Status
Update
Public Device Record Key
9614ea00-45bb-4590-9b79-ac66884308df

Device Description

PACKING 400407 MEROCEL 20PK PAIR BARON S

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
EFQ GAUZE/SPONGE, INTERNAL

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Unit of Use 00763000616779
Primary 20763000616773

Customer Contacts

Device Sizes

Type Value Unit Text
Width 2.0 Centimeter
Length 2.5 Centimeter
Height 1.2 Centimeter