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PF Targeting Module 125°

FDA UDI

Class II (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
PF Targeting Module 125° FDA UDI
Generic Name
Orthopaedic implant aiming arm FDA UDI
Device Name
PF Targeting Module 125° FDA UDI
Model / Reference
1F0I060A FDA UDI
Description
PF Targeting Module 125° FDA UDI

Identifiers

Catalog Number
1F0I060A FDA UDI
Primary DI / UDI-DI
09120116974109 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic implant aiming arm FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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: Orthopaedic implant aiming arm

PF Targeting Module 125° by I.T.S. GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant aiming arm.

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 7d02c4c6-7db1-4c94-a473-d93937b67c24 35 fields · synced Jun 8, 2026