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Tiger

FDA UDI

Class II (US FDA UDI)

by Trilliant Surgical LLC

Identity

Trade Name
Tiger FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
2.0MM x 40MM TIGER CANNULATED SCREW FDA UDI
Model / Reference
201-20-040 FDA UDI
Description
2.0MM x 40MM TIGER CANNULATED SCREW FDA UDI

Identifiers

Primary DI / UDI-DI
00810028398504 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Tiger by Trilliant Surgical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trilliant Surgical LLC

Sources (1)

  • FDA UDI c13e0295-ce63-41dd-b276-3d8fda91ce45 33 fields · synced May 31, 2026