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: Bone curette, reusable FDA UDI
Device Name: freshening instrument f 58.81.60 brown FDA UDI
Model / Reference: 58.82.07 FDA UDI
Description: freshening instrument f 58.81.60 brown FDA UDI

Identifiers

Catalog Number: 58.82.07 FDA UDI
Primary DI / UDI-DI: 04046826448486 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Bone curette, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Bone curette, reusable

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

Similar devices

Also classified as Bone curette, reusable.

Symmetry Bruns — SYMMETRY SURGICAL INC. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Spinal System — BIOMET SPINE LLC · Class I
Life Instruments — Life Instrument Corporation · Class I
Novo Surgical — NOVO SURGICAL, INC. · Class I
Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
Symmetry Meigs — SYMMETRY SURGICAL INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Medicon eG. Chirurgiemechaniker-Genossenschaft

Sources (1)

FDA UDI b7ee487f-a7cf-48ec-9e47-16e48535bf99 34 fields · synced Jun 8, 2026