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Harmonic HAR723

by Ethicon Endo-Surgery, LLC

Ref HAR723

Harmonic HAR723 is a device classified as Class IIb (EU), Unclassified (US) made by Ethicon Endo-Surgery, LLC, registered in EUDAMED on 13 May 2026 (Basic UDI-DI 0705036a000797D) and listed in FDA GUDID since 1 Mar 2024 (UDI-DI 10705036035763), 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 Number0705036a000797D Basic UDI-DI 10705036035763UDI-DIDate13 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10705036035763 UDI-DI Date1 Mar 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0705036a000797D registered 13 May 2026 Active
  • FDA GUDID UDI-DI 10705036035763 listed 1 Mar 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10705036035763
  2. Registered EUDAMED 0705036a000797D

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  • Withdrawn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
Harmonic
Generic name
Soft-tissue ultrasonic surgical system handpiece tip, single-use
Device name
HARMONIC 700 Shears
Model / Ref / Catalog
HAR723
Primary DI / UDI-DI
10705036035763
Basic UDI-DI
0705036a000797D
FDA product code
LFL
EMDN code
K0202010601, K0202010602
GMDN term
Soft-tissue ultrasonic surgical system handpiece tip, single-use
Device class
Class IIb EUDAMED
U GUDID
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
U

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

Related devices

Category: Soft-tissue ultrasonic surgical system handpiece tip, single-use

Similar devices in this category

Other devices filed under ULTRASONIC SURGERY INSTRUMENTS, SINGLE-USE.

Other devices from Ethicon Endo-Surgery, LLC

See all devices from Ethicon Endo-Surgery, LLC →

Properties

  • Supplied sterile
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)