FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00681490903004 · Model: 9560631 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00681490903004
Version / Model
9560631
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-08
Public Version
3
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
7390d672-b58f-45eb-9c93-5196e2736957

Device Description

INSTRUMENT 9560631 BAYON CUR 1.8MM RVRS

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
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00681490903004

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1.8mm