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PF Endcap, 0mm PPS

FDA UDI

Class II (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
PF Endcap, 0mm PPS FDA UDI
Generic Name
Bone nail end-cap FDA UDI
Device Name
PF Endcap, 0mm PPS FDA UDI
Model / Reference
1F0-10-30A-S FDA UDI
Description
PF Endcap, 0mm PPS FDA UDI

Identifiers

Catalog Number
1F0-10-30A-S FDA UDI
Primary DI / UDI-DI
09120116973867 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone nail end-cap 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

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bone nail end-cap

PF Endcap, 0mm PPS by I.T.S. GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone nail end-cap.

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 e1159857-55c3-4ed9-b2a3-418e55aa6707 35 fields · synced Jun 8, 2026