FDA UDI In Commercial Distribution 🇺🇸 United States

MESHGRAFT™

DI: 00889024372528 · Model: 00-2195-000-00 · ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MESHGRAFT™
Primary DI
00889024372528
Version / Model
00-2195-000-00
Catalog Number
00-2195-000-00
Company Name
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
Labeler DUNS
137354267
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-03
Public Version
1
Public Version Date
2021-03-11
Public Version Status
New
Public Device Record Key
68c785ef-d89b-4a0d-b527-6cec7195f0d3

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FZW EXPANDER, SURGICAL, SKIN GRAFT

GMDN Terms

Code Name
13614 Skin graft mesher

Identifiers

Type ID
Primary 00889024372528

Customer Contacts