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Aesculap AA846R

by Aesculap AG

Ref AA846R

Aesculap AA846R is a Class I device made by Aesculap AG, registered in EUDAMED on 19 Jan 2026 (Basic UDI-DI 40392390000005852S) and listed in FDA GUDID since 20 Apr 2020 (UDI-DI 04038653085101), active as of 12 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40392390000005852S Basic UDI-DI 04038653085101UDI-DIDate19 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653085101 UDI-DI Date20 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000005852S registered 19 Jan 2026 Active
  • FDA GUDID UDI-DI 04038653085101 listed 20 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653085101
  2. Registered EUDAMED 40392390000005852S

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  • Withdrawn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
Aesculap
Generic name
General-purpose calliper, metallic
Device name
Caliper Ir&m
Model / Ref / Catalog
AA846R
Primary DI / UDI-DI
04038653085101
Basic UDI-DI
40392390000005852S
Direct marketing DI
04038653085101
FDA product code
KTZ
EMDN code
V030201 Calipers
GMDN term
General-purpose calliper, metallic
Device class
Class I
Regulation number
888.4150
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under CALIPERS.

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Properties

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