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REMA Shaver Blades

FDA UDI

Class I (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
FULL-RADIUS-RESECTOR 4,2Ø MM, GEBOGEN FDA UDI
Model / Reference
15-60431 FDA UDI
Description
FULL-RADIUS-RESECTOR 4,2Ø MM, GEBOGEN FDA UDI

Identifiers

Catalog Number
15-60431 FDA UDI
Primary DI / UDI-DI
04059223160837 FDA UDI
FDA Product Code
HXR FDA UDI
GMDN Term
Arthroscopic shaver system blade, reusable 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

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 I — 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 97ca2098-9a5c-48c5-8bed-c33dbe583d75 34 fields · synced May 30, 2026