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Cortium Universal OCT Spinal Fixation System

FDA UDI

Class II (US FDA UDI)

by Ulrich Medical Usa, Inc.

Identity

Trade Name
Cortium Universal OCT Spinal Fixation System FDA UDI
Generic Name
Bone tap, single-use FDA UDI
Device Name
Tap, Ø 4.5mm, thoracic, AO coupling, cannulated, single use FDA UDI
Model / Reference
UU072-12-0145 FDA UDI
Description
Tap, Ø 4.5mm, thoracic, AO coupling, cannulated, single use FDA UDI

Identifiers

Primary DI / UDI-DI
00814386028295 FDA UDI
510(k) Number
K230614 FDA UDI
FDA Product Code
NKG FDA UDI
GMDN Term
Bone tap, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

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

Category: Bone tap, single-use

Cortium Universal OCT Spinal Fixation System by Ulrich Medical Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 442e16d7-d8c0-4748-a0b3-e5b096051bd4 35 fields · synced Jun 8, 2026