← Back to catalogue

Freedom Pneumatic Abdominal Compression Belt

EUDAMEDFDA UDI

Class I (EU MDR)

Ref Multiple COMP catalogue numbersModel Freedom Compression Belt Series

by CDR Systems Inc.

Identity

Trade Name
Freedom Pneumatic Abdominal Compression Belt EUDAMED
Freedom FDA UDI
Generic Name
Radiological compression belt FDA UDI
Device Name
Freedom Pneumatic Abdominal Compression Belt EUDAMED
Compression Belt FDA UDI
Model / Reference
Freedom Compression Belt Series EUDAMED
Multiple COMP catalogue numbers EUDAMED
1 FDA UDI
Description
Compression Belt FDA UDI

Identifiers

Catalog Number
COMP-KIT FDA UDI
Primary DI / UDI-DI
00628341930215 EUDAMEDFDA UDI
Basic UDI-DI
62834193058K EUDAMED
510(k) Number
K122888 FDA UDI
FDA Product Code
IYE FDA UDI
EMDN Code
Z12011280 PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Radiological compression belt FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Freedom Pneumatic Abdominal Compression Belt by CDR Systems Inc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
CDR Systems Inc.
EUDAMED SRN
CA-MF-000051790
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 1aad2af5-83e0-4fae-a783-083ceae81ed4 61 fields · synced Jun 18, 2026
  • FDA UDI 110a2d37-c2ad-4cef-a1cd-5a71d936c3d4 36 fields · synced May 30, 2026