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Pectus Bar, Universal 330 mm

FDA UDI

Class II (US FDA UDI)

by MedXpert GmbH

Identity

Trade Name
Pectus Bar, Universal 330 mm FDA UDI
Generic Name
Rib/rib cage internal fixation/bracing system bracing bar FDA UDI
Model / Reference
025-13330 FDA UDI

Identifiers

Primary DI / UDI-DI
04260029584202 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Rib/rib cage internal fixation/bracing system bracing bar 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 bracing bar

Pectus Bar, Universal 330 mm 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 bracing bar.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MedXpert GmbH

Sources (1)

  • FDA UDI 080b5010-2588-4b98-b995-80fce89f013c 32 fields · synced May 30, 2026