FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instruments

DI: 00763000070311 · Model: EX0917041 · 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
00763000070311
Version / Model
EX0917041
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-10
Public Version
1
Public Version Date
2022-10-18
Public Version Status
New
Public Device Record Key
fec15c7a-cfee-4f6e-802c-fed64de69372

Device Description

SPREADER EX0917041 CURVED ANTERIOR NARRW

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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
44378 Bone distraction forceps

Identifiers

Type ID
Primary 00763000070311

Customer Contacts