FDA UDI In Commercial Distribution 🇺🇸 United States

Endoskeleton™ TAS Interbody System

DI: 00763000512002 · Model: 687-030-102 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Endoskeleton™ TAS Interbody System
Primary DI
00763000512002
Version / Model
687-030-102
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-17
Public Version
3
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
e1bd2f7d-0703-46ab-8378-ca10f3991076

Device Description

TRAY 687-030-102 TAS ANTEROLATERAL INNER

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
LRP TRAY, SURGICAL

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00763000512002

Customer Contacts