FDA UDI In Commercial Distribution 🇺🇸 United States

Tornier Perform

DI: 03700386974571 · Model: MWE521 · TORNIER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tornier Perform
Primary DI
03700386974571
Version / Model
MWE521
Catalog Number
MWE521
Company Name
TORNIER
Labeler DUNS
260324876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-08
Public Version
1
Public Version Date
2022-08-16
Public Version Status
New
Public Device Record Key
90e35fbb-7a1c-4f72-a03d-2b6a04079642

Device Description

KEELED GLENOID TRIAL

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
Yes
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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 03700386974571

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: L40