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Compression Screw Instruments, For 3.5 mm Screws

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Compression Screw Instruments, For 3.5 mm Screws FDA UDI
Generic Name
Cannulated surgical drill bit, single-use FDA UDI
Model / Reference
130350oss FDA UDI

Identifiers

Catalog Number
THN00132 FDA UDI
Primary DI / UDI-DI
10818674027462 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Cannulated surgical drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Cannulated surgical drill bit, single-use

Compression Screw Instruments, For 3.5 mm Screws by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Cannulated surgical drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 694fda2a-fb9d-42ba-b34d-d31ed6e261f6 33 fields · synced May 30, 2026