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Friendship Medical

by Xi'an Friendship Medical Electronics Co., Ltd. 85 variants

Ref 3012Model PNHG2.0/80×2, PNHG, PNYG

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

CE MDR CE MDD

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 NumberB-16955739030129 Basic UDI-DI 16955739030129UDI-DIDate22 Feb 2022RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-16955739030129 Basic UDI-DI 16955739030129UDI-DIDate22 Feb 2022RegisteredStatusActive
United StatesGUDID listing GUDID Number16955739030129 UDI-DI Date17 Aug 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  • Withdrawn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, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Nerve-locating system probe, single-use
Device Name
Disposable Double Ball Tip Nerve Stimulator Probes
Model / Reference
PNHG2.0/80×2, 3012, PNHG, PNYG
Primary DI / UDI-DI
16955739030129
Basic UDI-DI
B-16955739030129, 695573903006LK
510(k) Number
FDA Product Code
ETN
EMDN Code
Z121002 Nervous system monitoring systems
GMDN Term
Nerve-locating system probe, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
874.1820
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000004202
Authorised representative
Friendship Europe ApS DK-AR-000001593

Other devices from Xi'an Friendship Medical Electronics Co., Ltd.

See all devices from Xi'an Friendship Medical Electronics Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No