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Cannulated Screw System +

FDA UDI

Class II (US FDA UDI)

by Tyber Medical

Identity

Trade Name
Cannulated Screw System + FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
5.5MM TI CANN SCREW +ST - 48MM-STER FDA UDI
Model / Reference
04.353.648TS FDA UDI
Description
5.5MM TI CANN SCREW +ST - 48MM-STER FDA UDI

Identifiers

Catalog Number
04.353.648TS FDA UDI
Primary DI / UDI-DI
00810040637131 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Cannulated Screw System + by Tyber Medical — 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
Tyber Medical

Sources (1)

  • FDA UDI 7278b688-59c5-4b29-aff3-89067e3767d4 35 fields · synced Jun 1, 2026