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REMA Shaver Blades

FDA UDI

Class II (US FDA UDI)

by DEWIMED Medizintechnik GmbH

Identity

Trade Name
REMA Shaver Blades FDA UDI
Generic Name
Arthroscopic shaver system blade, reusable FDA UDI
Device Name
MENISCUS CUTTER 3,4 Ø MM AUTOKLAVIERBAR FDA UDI
Model / Reference
15-60320 FDA UDI
Description
MENISCUS CUTTER 3,4 Ø MM AUTOKLAVIERBAR FDA UDI

Identifiers

Catalog Number
15-60320 FDA UDI
Primary DI / UDI-DI
04059223157783 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Arthroscopic shaver system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

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
Dry Heat Sterilization FDA UDI

Category: Arthroscopic shaver system blade, reusable

REMA Shaver Blades by DEWIMED Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DEWIMED Medizintechnik GmbH

Sources (1)

  • FDA UDI e6849e80-10c3-4e80-9a64-4c63eb6c40cf 34 fields · synced Jun 8, 2026