FDA UDI In Commercial Distribution 🇺🇸 United States

Made-To-Order

DI: 00846832099269 · Model: 9028051 · TORNIER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Made-To-Order
Primary DI
00846832099269
Version / Model
9028051
Catalog Number
9028051
Company Name
TORNIER, INC.
Labeler DUNS
968990812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-29
Public Version
3
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
dd9c1f26-0e3e-4012-a66d-6945c81d930c

Device Description

Ascend Flex Inlay Reamer

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
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
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00846832099269

Customer Contacts