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MediExpand Cervical Expandable VBR System

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
MediExpand Cervical Expandable VBR System FDA UDI
Generic Name
Medical ruler, reusable FDA UDI
Device Name
ruler f length gauge 58.81.99 FDA UDI
Model / Reference
58.82.21 FDA UDI
Description
ruler f length gauge 58.81.99 FDA UDI

Identifiers

Catalog Number
58.82.21 FDA UDI
Primary DI / UDI-DI
04046826468255 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Medical ruler, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Medical ruler, reusable

MediExpand Cervical Expandable VBR System by Medicon eG. Chirurgiemechaniker-Genossenschaft — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Medical ruler, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6cef759-dd40-468e-a087-b9a9078f6a6a 34 fields · synced Jun 8, 2026