FDA UDI In Commercial Distribution 🇺🇸 United States

TM Reverse Shoulder

DI: 00889024569232 · Model: 82-0180-125-00 · Zimmer, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TM Reverse Shoulder
Primary DI
00889024569232
Version / Model
82-0180-125-00
Catalog Number
82-0180-125-00
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-18
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
d119d49a-ddd9-451d-aa29-9e2171157d10

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
Yes
Has Lot/Batch Number
No
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
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00889024569232

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 7.5 mm Diameter x 15 mm Length