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Aesculap EM710R

by Aesculap AG

Ref EM710R

Aesculap EM710R is a surgical soft-tissue manipulation forceps (EU MDR Class I; FDA Class I; FDA product code HDF, Speculum, Vaginal, Metal) made by Aesculap AG, registered in EUDAMED on 19 Jan 2026 (Basic UDI-DI 40392390000006152A) and listed in FDA GUDID since 20 Apr 2020 (UDI-DI 04038653041237), 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 Number40392390000006152A Basic UDI-DI 04038653041237UDI-DIDate19 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653041237 UDI-DI Date20 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000006152A registered 19 Jan 2026 Active
  • FDA GUDID UDI-DI 04038653041237 listed 20 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653041237
  2. Registered EUDAMED 40392390000006152A

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  • Withdrawn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
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device name
Cervix/urethra endospeculum
Model / Ref / Catalog
EM710R
Primary DI / UDI-DI
04038653041237
Basic UDI-DI
40392390000006152A
Direct marketing DI
04038653041237
FDA product code
HDF
EMDN code
L0509020299 Gynecological use spreaders, reusable - other
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class I
Regulation number
884.4520
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under GYNECOLOGICAL USE DILATORS AND SPREADERS, REUSABLE.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)