← Back to catalogue

Medicon

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
General-purpose surgical spatula FDA UDI
Device Name
Legueu bladder retr 25x105mm 25cm FDA UDI
Model / Reference
51.81.15 FDA UDI
Description
Legueu bladder retr 25x105mm 25cm FDA UDI

Identifiers

Catalog Number
51.81.15 FDA UDI
Primary DI / UDI-DI
04046826063146 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
General-purpose surgical spatula 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: General-purpose surgical spatula

Medicon by Medicon eG. Chirurgiemechaniker-Genossenschaft — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical spatula.

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

Sources (1)

  • FDA UDI 95c7aca7-8dba-4ff3-8130-f9b0eac5c1ec 35 fields · synced May 30, 2026