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BodyFIX Manifold Tube 1500 mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref P10102-212

by 3C-Medical Intelligence GmbH

Identity

Trade Name
BodyFIX Manifold Tube 1500 mm EUDAMED
BodyFIX FDA UDI
Generic Name
Vacuum-mould patient positioning system FDA UDI
Device Name
BodyFIX, BlueBAG EUDAMED
Together with the Manifold Cushion the BodyFIX® Manifold Tube 1500mm establishes a permanent and equal vacuum over the patient. FDA UDI
Model / Reference
P10102-212 EUDAMEDFDA UDI
Description
Together with the Manifold Cushion the BodyFIX® Manifold Tube 1500mm establishes a permanent and equal vacuum over the patient. FDA UDI

Identifiers

Catalog Number
P10102-212 FDA UDI
Primary DI / UDI-DI
04056719000141 EUDAMEDFDA UDI
Basic UDI-DI
04056719BUDI0000000001HU EUDAMED
Direct Marketing DI
04056719000141 EUDAMED
510(k) Number
K121530 FDA UDI
FDA Product Code
IYE FDA UDI
EMDN Code
V0804 PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures) EUDAMED
GMDN Term
Vacuum-mould patient positioning system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Market of Registration
Germany 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

BodyFIX Manifold Tube 1500 mm by 3C-Medical Intelligence GmbH — 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

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Manufacturer

Manufacturer
3C-Medical Intelligence GmbH
EUDAMED SRN
DE-MF-000023763

Sources (3)

  • EUDAMED 1d8c49b5-2c56-4b2d-9b28-e5089d4c055e 61 fields · synced Jun 18, 2026
  • FDA UDI 58f4bbc0-dc6c-4b3b-a18d-b4a3b8ac1f81 35 fields · synced May 30, 2026
  • EUDAMED 85c6e3b5-9fc4-4814-9f88-8527a16ecae0 61 fields · synced Jun 11, 2026