← Back to catalogue

Titanium 3D rib clip, 13 segments

FDA UDI

Class II (US FDA UDI)

by MedXpert GmbH

Identity

Trade Name
Titanium 3D rib clip, 13 segments FDA UDI
Generic Name
Rib/rib cage internal fixation/bracing system fixation grip/anchor FDA UDI
Model / Reference
014-01013 FDA UDI

Identifiers

Catalog Number
014-01013 FDA UDI
Primary DI / UDI-DI
04260029583403 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Rib/rib cage internal fixation/bracing system fixation grip/anchor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Rib/rib cage internal fixation/bracing system fixation grip/anchor

Titanium 3D rib clip, 13 segments by MedXpert GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rib/rib cage internal fixation/bracing system fixation grip/anchor.

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
MedXpert GmbH

Sources (1)

  • FDA UDI 08fda55d-3a96-4ba3-9ad1-ce8742c45559 34 fields · synced May 30, 2026