FDA UDI In Commercial Distribution 🇺🇸 United States

Tornier Perform

DI: 03700386973536 · Model: MWE101 · TORNIER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tornier Perform
Primary DI
03700386973536
Version / Model
MWE101
Catalog Number
MWE101
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
3e7ce86d-3bb1-48bb-af61-70e9bc6b7949

Device Description

Keeled Punch

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
LRY PUNCH, SURGICAL

GMDN Terms

Code Name
64337 Bone-coring punch, reusable

Identifiers

Type ID
Primary 03700386973536

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: Small/Medium