Skip to content

Emprint CA190RC1

by Covidien LP

Ref CA190RC1

Emprint CA190RC1 is an electrical-only medical device connection cable (EU MDR Class I; FDA Class II) made by Covidien LP, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI 0763000B00001016M) and listed in FDA GUDID since 1 Aug 2017 (UDI-DI 10884521190764), 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 Number0763000B00001016M Basic UDI-DI 10884521190764UDI-DIDate6 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10884521190764 UDI-DI Date1 Aug 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0763000B00001016M registered 6 Nov 2026 Active
  • FDA GUDID UDI-DI 10884521190764 listed 1 Aug 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10884521190764
  2. Registered EUDAMED 0763000B00001016M

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  • Withdrawn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
Emprint™ EUDAMED
Emprint GUDID
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
CA190RC1
Primary DI / UDI-DI
10884521190764
Basic UDI-DI
0763000B00001016M
FDA product code
GEI, NEY
EMDN code
L1899 Electrosurgery instruments, reusable - other
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4400
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Length — 190 Centimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Covidien LP

  • LigaSure MRASILF19

    Class II

  • Shiley 110860

    Class II

  • Shiley 110865

    Class II

  • Shiley 110870

    Class II

See all devices from Covidien LP →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)