FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instruments

DI: 00681490542234 · Model: 9116882 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic Reusable Instruments
Primary DI
00681490542234
Version / Model
9116882
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-26
Public Version
1
Public Version Date
2022-12-05
Public Version Status
New
Public Device Record Key
5f8d623d-88d3-4dc2-969f-b4c338815182

Device Description

INSTRUMENT 9116882 AR I V D RR 7MM12MMCP

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
No
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
HTX RONGEUR

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00681490542234

Customer Contacts