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Perla ® Tl Nav Nav-Bx 40 00-N

by Spineart

Ref NAV-BX 40 00-N

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number1764045086SRI02REUSIN012R Basic UDI-DIDate23 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640221373656 UDI-DIDate13 Apr 2026ListedStatusListed 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.

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  • Withdrawn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
Perla® Tl Nav Perla Tl Pilot Hole Navigation Instrument Box EUDAMED
Perla ® Tl Nav GUDID
Generic Name
Instrument tray, reusable
Device Name
Reusable Instruments I Boxes
Model / Ref / Catalog
NAV-BX 40 00-N
Primary DI / UDI-DI
07640221373656
Basic UDI-DI
1764045086SRI02REUSIN012R
Direct Marketing DI
07640221373656
FDA Product Code
FSM
EMDN Code
S010401 Trays, baskets, tubs for sterilisation and their components
GMDN Term
Instrument tray, reusable
Device Class
Class I
Regulation Number
878.4800
Market of Registration
France
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Spineart

See all devices from Spineart →

Properties

  • Reusable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: 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
  • Serial Number: No
  • Expiration Date: No