FDA UDI In Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TT

DI: 00191375003045 · Model: 4200-1017 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TT
Primary DI
00191375003045
Version / Model
4200-1017
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
6
Public Version Date
2021-04-01
Public Version Status
Update
Public Device Record Key
5253b36e-1388-4c5f-a405-15d9cf90ccda

Device Description

Large Angled Right Curette

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
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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00191375003045

Customer Contacts

Device Sizes

Type Value Unit Text
Length 14 Inch