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Tryptik ® Ti

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name
TRYPTIK ® TI FDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
ANATOMIC RASP TRIAL SMALL H10 FDA UDI
Model / Reference
TRY-00 RS 10-N FDA UDI
Description
ANATOMIC RASP TRIAL SMALL H10 FDA UDI

Identifiers

Catalog Number
TRY-00 RS 10-N FDA UDI
Primary DI / UDI-DI
07640450863560 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 10 Millimeter FDA UDI

Category: Spinal implant trial

Tryptik ® Ti by Spineart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal implant trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spineart

Sources (1)

  • FDA UDI 623c01b0-fb6a-4a3f-ac0d-b162bb09fa60 35 fields · synced May 31, 2026