FDA UDI In Commercial Distribution 🇺🇸 United States

Fitmore®

DI: 00889024470682 · Model: 01.00555.111 · Zimmer GmbH
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fitmore®
Primary DI
00889024470682
Version / Model
01.00555.111
Catalog Number
01.00555.111
Company Name
Zimmer GmbH
Labeler DUNS
488133448
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-13
Public Version
7
Public Version Date
2023-06-27
Public Version Status
Update
Public Device Record Key
83f35cfe-8b33-4735-afb8-b12aff3b6183

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
No
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
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
KWL Prosthesis, hip, hemi-, femoral, metal
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00889024470682

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 0mm provisional rasp, A/11