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Bending cylinder for Pectus bars, 13.7 mm supplement for 020-00021

FDA UDI

Class I (US FDA UDI)

by MedXpert GmbH

Identity

Trade Name
Bending cylinder for Pectus bars, 13.7 mm supplement for 020-00021 FDA UDI
Generic Name
Rib/rib cage internal fixation/bracing system bending pliers FDA UDI
Model / Reference
020-00029 FDA UDI

Identifiers

Catalog Number
020-00029 FDA UDI
Primary DI / UDI-DI
04260029580167 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Rib/rib cage internal fixation/bracing system bending pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Rib/rib cage internal fixation/bracing system bending pliers

Bending cylinder for Pectus bars, 13.7 mm supplement for 020-00021 by MedXpert GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rib/rib cage internal fixation/bracing system bending pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MedXpert GmbH

Sources (1)

  • FDA UDI a2ac3749-8894-4e71-8883-79bf1e5c98f3 34 fields · synced May 30, 2026