Skip to content

Medical Dermatome Blade

by Jiangsu MJD Medical Technology Co., Ltd. 22 variants

Ref MT-B-90Model MT

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Overview

The Medical Dermatome Blade is a versatile and innovative medical device designed for precise skin mapping and treatment. Its advanced technology enables accurate and reliable dermatological analysis, making it an essential tool in various medical specialties.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number6975808860001FV Basic UDI-DI 06975808863062UDI-DIDate3 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06975808863062 UDI-DI Date28 Nov 2025ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Medical Dermatome Blade EUDAMED
Mt GUDID
Generic Name
Dermatome blade, single-use
Model / Reference
MT, MT-B-90
Primary DI / UDI-DI
06975808863062
Basic UDI-DI
6975808860001FV
FDA Product Code
GFD
EMDN Code
V010302 Blades without safety systems, single-use - not included in other classes
GMDN Term
Dermatome blade, single-use
Device Class
Class I
Regulation Number
878.4820
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
CN-MF-000051652
Authorised representative
Humiss International B.V. NL-AR-000001490

Related devices

Category: Manual scalpel blade, single-use

Other devices from Jiangsu Mjd Medical Technology Co., Ltd.

See all devices from Jiangsu Mjd Medical Technology Co., Ltd. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No