FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00643169332362 · Model: X1012025 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00643169332362
Version / Model
X1012025
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-10
Public Version
3
Public Version Date
2023-10-31
Public Version Status
Update
Public Device Record Key
52235b98-0d37-45ed-9d27-6c899804c53a

Device Description

PITUITARY X1012025 4MM STRAIGHT

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00643169332362

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 4mm