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PF Lag Screw Driver Retaining Rod

FDA UDI

Class I (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
PF Lag Screw Driver Retaining Rod FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
PF Lag Screw Driver Retaining Rod FDA UDI
Model / Reference
1F0I160A FDA UDI
Description
PF Lag Screw Driver Retaining Rod FDA UDI

Identifiers

Catalog Number
1F0I160A FDA UDI
Primary DI / UDI-DI
09120116974734 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical screwdriver, reusable 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

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

Category: Surgical screwdriver, reusable

PF Lag Screw Driver Retaining Rod by I.T.S. GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I.T.S. GmbH

Sources (1)

  • FDA UDI a8932429-385d-41b8-89c1-68ab0fd95557 35 fields · synced Jun 8, 2026