FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00673978050195 · Model: 830-150 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00673978050195
Version / Model
830-150
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-17
Public Version
5
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
035f56a9-b99f-4112-84a5-db87fff4156d

Device Description

INSTRUMENT 830-150 DRILL GUIDE LEFT

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00673978050195

Customer Contacts