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FeetSupport™, fixed 2.0

FDA UDI

Class II (US FDA UDI)

by Macromedics B.v.

Identity

Trade Name
FeetSupport™, fixed 2.0 FDA UDI
Generic Name
Indexed-immobilization patient positioning system FDA UDI
Device Name
FeetSupport 2.0, fixed, 3P FDA UDI
Model / Reference
FSTSF2.0 FDA UDI
Description
FeetSupport 2.0, fixed, 3P FDA UDI

Identifiers

Catalog Number
130450 FDA UDI
Primary DI / UDI-DI
08720168160362 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Indexed-immobilization patient positioning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Indexed-immobilization patient positioning system

FeetSupport™, fixed 2.0 by Macromedics B.v. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indexed-immobilization patient positioning system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Macromedics B.v.

Sources (1)

  • FDA UDI 45b0f15f-855b-4629-911b-caf58f1e4072 34 fields · synced May 30, 2026