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INSTRUMENTS - Disc Hernia Forceps

by NovaSpine 98 variants

Ref NRBS-180-4-S

INSTRUMENTS - Disc Hernia Forceps (NRBS-180-4-S) is a Class I device made by NovaSpine, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 37004822INSTRUMENT138U), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37004822INSTRUMENT138U Basic UDI-DI 03700482266723UDI-DIDate4 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
INSTRUMENTS - Disc Hernia Forceps
Model / reference
NRBS-180-4-S
Primary DI / UDI-DI
03700482266723
Basic UDI-DI
37004822INSTRUMENT138U
Direct marketing DI
03700482266723
EMDN code
L110601 Disc hernia forceps, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000007304

Other devices from NovaSpine

See all devices from NovaSpine →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)