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Medicon

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
Cast/plaster knife FDA UDI
Device Name
Engel plaster saw 15cm FDA UDI
Model / Reference
40.66.05 FDA UDI
Description
Engel plaster saw 15cm FDA UDI

Identifiers

Catalog Number
40.66.05 FDA UDI
Primary DI / UDI-DI
04046826045074 FDA UDI
FDA Product Code
LGG FDA UDI
GMDN Term
Cast/plaster knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5980 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: Cast/plaster knife

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

Similar devices

Also classified as Cast/plaster knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c5fdda84-40d3-4f2e-b42e-22e05ae94685 35 fields · synced Jun 1, 2026