FDA UDI In Commercial Distribution 🇺🇸 United States

Tornier Flex

DI: 03700386972867 · Model: MWE002 · TORNIER
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tornier Flex
Primary DI
03700386972867
Version / Model
MWE002
Catalog Number
MWE002
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
ba0bbd04-461d-4d7f-ad26-58d6e0cd0e4b

Device Description

HUMERAL HEAD TRIAL SCREW

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
Yes
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
47779 Orthopaedic instrument surgical connector

Identifiers

Type ID
Primary 03700386972867

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size: 2