Skip to content

NEAL Pre-cut Splint N

by BL Tech 9 variants

Ref NHPS-5050N, NHPS-5050-NModel NHRS, NHPS - F/G, SP, NW, NEAL SPLINT, Pre-cut

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880927046SPLINTVM Basic UDI-DI 08809270467641UDI-DIDate1 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
NEAL Pre-cut Splint N
Neal Splint precut N 12,5x125cm
Device Name
Nhrs, Nhps - F/G, Sp, Nw
Model / Reference
NHRS, NHPS - F/G, SP, NW, NHPS-5050N, NEAL SPLINT, Pre-cut, NHPS-5050-N
Primary DI / UDI-DI
08809270467641
Basic UDI-DI
880927046SPLINTVM, 880927046SPLINTPRECUTDX
EMDN Code
M030504, M03050202
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
KR-MF-000013035
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from BL Tech

See all devices from BL Tech →

Properties

Other properties (13)

  • Sterile: 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No