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Evolution E1500040

by MicroPort Orthopedics Inc.

Ref E1500040

Evolution E1500040 is a Class I device made by MicroPort Orthopedics Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 0192629IRKV030201BV) and listed in FDA GUDID since 23 Dec 2019 (UDI-DI 00192629232020), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0192629IRKV030201BV Basic UDI-DI 00192629232020UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00192629232020 UDI-DI Date23 Dec 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0192629IRKV030201BV registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 00192629232020 listed 23 Dec 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00192629232020
  2. Registered EUDAMED 0192629IRKV030201BV

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  • Withdrawn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
Evolution® Ka Cartilage Thickness Gauge EUDAMED
Evolution GUDID
Generic name
Surgical depth gauge, reusable
Device name
Knee CALIPERS
Model / Ref / Catalog
E1500040
Primary DI / UDI-DI
00192629232020 EUDAMED
M684E15000401 GUDID
Basic UDI-DI
0192629IRKV030201BV
Secondary DI
M684E15000401
Direct marketing DI
00192629232020
FDA product code
HTJ
EMDN code
V030201 Calipers
GMDN term
Surgical depth gauge, reusable
Device class
Class I
Regulation number
888.4300
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00192629232020
GUDID
M684E15000401

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00192629232020; FDA GUDID lists M684E15000401), so their flags are not compared.

Related devices

Category: Surgical depth gauge, reusable

Similar devices in this category

Other devices filed under CALIPERS.

Other devices from MicroPort Orthopedics Inc.

See all devices from MicroPort Orthopedics Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)