FDA UDI In Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TAS

DI: 00191375028697 · Model: 2312-9110 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TAS
Primary DI
00191375028697
Version / Model
2312-9110
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-30
Public Version
3
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
8fbf4676-b923-474c-93c0-45a1cb460db4

Device Description

Trial, Anterolateral, 12 Deg Lordotic, Standard, 10mm

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
HWT TEMPLATE

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00191375028697

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify width(MLxAP), 32 x 21, mm
Angle 7 degree
Width 32 Millimeter
Device Size Text, specify Lordotic Angle 12 Deg
Height 10 Millimeter
Depth 21 Millimeter