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CT HeadFix

FDA UDI

Class I (US FDA UDI)

by Pearl Technology AG

Identity

Trade Name
CT HeadFix FDA UDI
Generic Name
Radiological headrest FDA UDI
Device Name
Positioning aid for head fixation in the CT head holder. FDA UDI
Model / Reference
CT HeadFix FDA UDI
Description
Positioning aid for head fixation in the CT head holder. FDA UDI

Identifiers

Catalog Number
1105 FDA UDI
Primary DI / UDI-DI
07640178060081 FDA UDI
FDA Product Code
IWY FDA UDI
GMDN Term
Radiological headrest FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1920 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiological headrest

CT HeadFix by Pearl Technology AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological headrest.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pearl Technology AG

Sources (1)

  • FDA UDI 3197b4c6-0596-4d60-a5a8-4b18d8628b7b 35 fields · synced Jun 6, 2026