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Rongeurs

by Life Instrument Corporation

Ref 730-0801-0

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++M930003PX Basic UDI-DI M930730080100UDI-DIDate31 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberM930730080100 UDI-DI Date27 Nov 2023ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Life Instruments
Generic Name
Orthopaedic joint/limb rongeur
Spinal rongeur
Device Name
Rongeurs
Model / Reference
730-0801-0 EUDAMED
832-0722-0 GUDID
831-1232-3 GUDID
830-1004-1 GUDID
831-1002-0 GUDID
832-0702-0 GUDID
873-1304-0 GUDID
831-1003-0 GUDID
830-0802-0 GUDID
832-0904-2 GUDID
838-0815-0 GUDID
837-8002-0 GUDID
837-1015-0 GUDID
837-0903-1 GUDID
836-9505-1 GUDID
732-8050-2 GUDID
831-1005-0T GUDID
830-0806-1 GUDID
831-0703-1 GUDID
837-8111-0 GUDID
834-0703-1 GUDID
830-1202-1 GUDID
839-0602-0T GUDID
830-0802-1 GUDID
838-1012-0A GUDID
831-1034-0 GUDID
831-1024-0 GUDID
839-5502-1 GUDID
832-0703-2 GUDID
831-0804-1 GUDID
831-0804-2 GUDID
873-1506-0 GUDID
836-1212-0 GUDID
838-0711-0 GUDID
839-0601-1 GUDID
830-0804-0AB GUDID
732-1240-0 GUDID
839-5502-0TS GUDID
837-8001-0 GUDID
830-0803-2 GUDID
830-1204-0 GUDID
830-1003-0A GUDID
839-0802-1B GUDID
830-1001-2 GUDID
839-0715-3 GUDID
830-0813-0 GUDID
834-0902-0 GUDID
830-1033-0 GUDID
831-0803-0 GUDID
732-1220-0 GUDID
838-0805-0B GUDID
Primary DI / UDI-DI
M930730080100 EUDAMED
M930832072200 GUDID
M930831123230 GUDID
M930830100410 GUDID
M930831100200 GUDID
M930832070200 GUDID
M930873130400 GUDID
M930831100300 GUDID
M930830080200 GUDID
M930832090420 GUDID
M930838081500 GUDID
M930837800200 GUDID
M930837101500 GUDID
M930837090310 GUDID
M930836950510 GUDID
M930732805020 GUDID
M93083110050T0 GUDID
M930830080610 GUDID
M930831070310 GUDID
M930837811100 GUDID
M930834070310 GUDID
M930830120210 GUDID
M93083906020T0 GUDID
M930830080210 GUDID
M93083810120A0 GUDID
M930831103400 GUDID
M930831102400 GUDID
M930839550210 GUDID
M930832070320 GUDID
M930831080410 GUDID
M930831080420 GUDID
M930873150600 GUDID
M930836121200 GUDID
M930838071100 GUDID
M930839060110 GUDID
M93083008040AB0 GUDID
M930732124000 GUDID
M93083955020TS0 GUDID
M930837800100 GUDID
M930830080320 GUDID
M930830120400 GUDID
M93083010030A0 GUDID
M93083908021B0 GUDID
M930830100120 GUDID
M930839071530 GUDID
M930830081300 GUDID
M930834090200 GUDID
M930830103300 GUDID
M930831080300 GUDID
M930732122000 GUDID
M93083808050B0 GUDID
Basic UDI-DI
++M930003PX
Direct Marketing DI
M930730080100
FDA Product Code
HTX
EMDN Code
L091302, L110604
GMDN Term
Orthopaedic joint/limb rongeur
Spinal rongeur
Device Class
Class I
Regulation Number
888.4540
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
730-0801-0
GUDID
832-0722-0
831-1232-3
830-1004-1
831-1002-0
832-0702-0
873-1304-0
831-1003-0
830-0802-0
832-0904-2
838-0815-0
837-8002-0
837-1015-0
837-0903-1
836-9505-1
732-8050-2
831-1005-0T
830-0806-1
831-0703-1
837-8111-0
834-0703-1
830-1202-1
839-0602-0T
830-0802-1
838-1012-0A
831-1034-0
831-1024-0
839-5502-1
832-0703-2
831-0804-1
831-0804-2
873-1506-0
836-1212-0
838-0711-0
839-0601-1
830-0804-0AB
732-1240-0
839-5502-0TS
837-8001-0
830-0803-2
830-1204-0
830-1003-0A
839-0802-1B
830-1001-2
839-0715-3
830-0813-0
834-0902-0
830-1033-0
831-0803-0
732-1220-0
838-0805-0B
Primary DI / UDI-DIEUDAMED
M930730080100
GUDID
M930832072200
M930831123230
M930830100410
M930831100200
M930832070200
M930873130400
M930831100300
M930830080200
M930832090420
M930838081500
M930837800200
M930837101500
M930837090310
M930836950510
M930732805020
M93083110050T0
M930830080610
M930831070310
M930837811100
M930834070310
M930830120210
M93083906020T0
M930830080210
M93083810120A0
M930831103400
M930831102400
M930839550210
M930832070320
M930831080410
M930831080420
M930873150600
M930836121200
M930838071100
M930839060110
M93083008040AB0
M930732124000
M93083955020TS0
M930837800100
M930830080320
M930830120400
M93083010030A0
M93083908021B0
M930830100120
M930839071530
M930830081300
M930834090200
M930830103300
M930831080300
M930732122000
M93083808050B0

Manufacturer details

EUDAMED SRN
US-MF-000043403
Authorised representative
MedEnvoy Global BV NL-AR-000024028

Other devices from Life Instrument Corporation

See all devices from Life Instrument Corporation →

Properties

  • Reusable
  • Premarket Exempt

Other properties (22)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No