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Pnp Tibia 01-1540-7000

by Orthopediatrics Corp.

Part of a family of 52 devices: see the family page

Ref 01-1540-7000Model 01-1501-0090

Pnp Tibia 01-1540-7000 is a device classified as Class IIa in the EU and Class I in the US made by Orthopediatrics Corp., registered in EUDAMED on 29 May 2026 (Basic UDI-DI 08411321CIIAREAMAR) and listed in FDA GUDID since 11 Sep 2024 (UDI-DI 00840194467131), 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 Number08411321CIIAREAMAR Basic UDI-DI 00840194467131UDI-DIDate29 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00840194467131 UDI-DI Date11 Sep 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08411321CIIAREAMAR registered 29 May 2026 Active
  • FDA GUDID UDI-DI 00840194467131 listed 11 Sep 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00840194467131
  2. Registered EUDAMED 08411321CIIAREAMAR

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  • Withdrawn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
Orthopediatrics® Instrumentation EUDAMED
Pnp Tibia GUDID
Generic name
Medullary canal orthopaedic reamer, flexible
Model / Ref / Catalog
01-1540-7000, 01-1501-0090
Primary DI / UDI-DI
00840194467131
Basic UDI-DI
08411321CIIAREAMAR
FDA product code
KIJ
EMDN code
P0999 Orthopaedic prostheses, osteosynthesis devices, devices for tendon and ligament synthesis - other
GMDN term
Medullary canal orthopaedic reamer, flexible
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

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

Related devices

Category: Medullary canal orthopaedic reamer, flexible

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES, OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS - OTHER.

Other devices from Orthopediatrics Corp.

See all devices from Orthopediatrics Corp. →

Properties

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