← Back to catalogue

Medicon

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
Skin staple remover, reusable FDA UDI
Device Name
Hernandez Ros staple extractor 19cm FDA UDI
Model / Reference
76.09.09 FDA UDI
Description
Hernandez Ros staple extractor 19cm FDA UDI

Identifiers

Catalog Number
76.09.09 FDA UDI
Primary DI / UDI-DI
04046826148195 FDA UDI
FDA Product Code
HXW FDA UDI
GMDN Term
Skin staple remover, 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Skin staple remover, reusable

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

Similar devices

Also classified as Skin staple remover, reusable.

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

Manufacturer
Medicon eG. Chirurgiemechaniker-Genossenschaft

Sources (1)

  • FDA UDI f122ff65-76f8-4912-9868-4b15855e42f6 35 fields · synced May 30, 2026