FDA UDI Not in Commercial Distribution 🇺🇸 United States

DRLock Extreme™

DI: 00846832031191 · Model: DRE-002-0NR · TORNIER, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DRLock Extreme™
Primary DI
00846832031191
Version / Model
DRE-002-0NR
Catalog Number
DRE-002-0NR
Company Name
TORNIER, INC.
Labeler DUNS
968990812
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-16
Public Version
6
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
4a4b0d4c-7a0d-44b8-ace6-373edca4bdea
Distribution End Date
2022-11-01

Device Characteristics

Single Use
Yes
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
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
HRS PLATE, FIXATION, BONE
HWC Screw, fixation, bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00846832031191

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size Narrow Width Short Length