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Pulse Oximeter

by Shenzhen Jumper Medical Equipment Co., Ltd 11 variants

Ref JPD-500E

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number69517405SP01TL Basic UDI-DI 06951740540285UDI-DIDate28 May 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number06951740540285 UDI-DI Date24 Sep 2016ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
Pulse Oximeter EUDAMED
pluse oximeter GUDID
Generic Name
Pulse oximeter
Model / Reference
JPD-500E EUDAMED
JPD-500A GUDID
Primary DI / UDI-DI
06951740540285 EUDAMED
06951740500173 GUDID
Basic UDI-DI
69517405SP01TL
Direct Marketing DI
06951740540285
510(k) Number
FDA Product Code
DQA
EMDN Code
Z1203020408 Pulse oximeters
GMDN Term
Pulse oximeter
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.2700
EU market of registration
Lithuania
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
JPD-500E
GUDID
JPD-500A
Primary DI / UDI-DIEUDAMED
06951740540285
GUDID
06951740500173
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000014343
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Shenzhen Jumper Medical Equipment Co., Ltd

See all devices from Shenzhen Jumper Medical Equipment Co., Ltd →

Properties

  • Measuring Function
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No