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Tryptik 2 C-Plate Instrumentation Try-in 06 32-N

by Spineart

Ref TRY-IN 06 32-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 Number1764045086SRI01REUSIN2A36 Basic UDI-DI 07640178983281UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07640178983281 UDI-DI Date1 Aug 2018ListedStatusListed 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  • Withdrawn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
TRYPTIK®2 C-Plate Plate Template 2 Level EUDAMED
Tryptik 2 C-Plate Instrumentation GUDID
Generic Name
Spinal implant trial
Device Name
SURGICAL REUSABLE INSTRUMENTS IIa
Model / Ref / Catalog
TRY-IN 06 32-N
Primary DI / UDI-DI
07640178983281
Basic UDI-DI
1764045086SRI01REUSIN2A36
Direct Marketing DI
07640178983281
FDA Product Code
HWT
EMDN Code
L091099 Osteosynthesis instruments, reusable - other
GMDN Term
Spinal implant trial
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
888.4800
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I

Related devices

Category: Spinal implant trial

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