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Aesculap OL451R

by Aesculap, Inc.

Ref OL451R

Aesculap OL451R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 13 Oct 2025 (Basic UDI-DI 4039239000001306ZW) and listed in FDA GUDID since 22 Apr 2020 (UDI-DI 04038653178605), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000001306ZW Basic UDI-DI 04038653178605UDI-DIDate13 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653178605 UDI-DI Date22 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000001306ZW registered 13 Oct 2025 Active
  • FDA GUDID UDI-DI 04038653178605 listed 22 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653178605
  2. Registered EUDAMED 4039239000001306ZW

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  • Withdrawn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
Manual surgical saw, rigid
Device name
Nasal saw
Model / Ref / Catalog
OL451R
Primary DI / UDI-DI
04038653178605
Basic UDI-DI
4039239000001306ZW
Direct marketing DI
04038653178605
FDA product code
KBC
EMDN code
L010701 Manual surgical saws, reusable
GMDN term
Manual surgical saw, rigid
Device class
Class I
Regulation number
874.4420
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 SHARP INSTRUMENTS, REUSABLE.

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)