← Back to catalogue

Endoskeleton® Tas

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
ENDOSKELETON® TAS FDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
Trial, Anterolateral, 12 Deg Lordotic, Large, 11mm FDA UDI
Model / Reference
2312-9211 FDA UDI
Description
Trial, Anterolateral, 12 Deg Lordotic, Large, 11mm FDA UDI

Identifiers

Primary DI / UDI-DI
00191375028802 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Angle — 7 degree FDA UDI
Depth — 24 Millimeter FDA UDI
Height — 11 Millimeter FDA UDI
Width — 36 Millimeter FDA UDI

Category: Spinal implant trial

Endoskeleton® Tas by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal implant trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtronic Sofamor Danek, Inc.

Sources (1)

  • FDA UDI e7176700-fc0c-4166-9af8-825a4de58d18 35 fields · synced Jun 1, 2026