FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instrument

DI: 20673978069160 · Model: 875-089 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Medtronic Reusable Instrument
Primary DI
20673978069160
Version / Model
875-089
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-10-15
Public Version
1
Public Version Date
2022-10-24
Public Version Status
New
Public Device Record Key
7c7f254d-e49b-41f5-9e1c-af5fe60630b7

Device Description

DISTRACTOR 875-089 PINS 16MM

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Unit of Use 00673978069166
Primary 20673978069160

Customer Contacts