← Back to catalogue

BodyFIX

FDA UDI

Class II (US FDA UDI)

by 3C-Medical Intelligence GmbH

Identity

Trade Name
BodyFIX FDA UDI
Generic Name
Stereotactic radiosurgical/radiotherapy arch head frame FDA UDI
Device Name
BlueBAG™ HeadFIX® T-Shape 850x800mm/16,5L custom-formed vacuum cushion provides comfortable support for the head. FDA UDI
Model / Reference
P10104-605 FDA UDI
Description
BlueBAG™ HeadFIX® T-Shape 850x800mm/16,5L custom-formed vacuum cushion provides comfortable support for the head. FDA UDI

Identifiers

Catalog Number
P10104-605 FDA UDI
Primary DI / UDI-DI
04056719000752 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Stereotactic radiosurgical/radiotherapy arch head frame FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

BodyFIX by 3C-Medical Intelligence GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d28b1a73-b4a7-4004-b00c-31a6a35c4b0e 35 fields · synced May 30, 2026