FDA UDI In Commercial Distribution 🇺🇸 United States

BodyFIX

DI: 04056719001940 · Model: P10102-233 · 3C-Medical Intelligence GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BodyFIX
Primary DI
04056719001940
Version / Model
P10102-233
Catalog Number
P10102-233
Company Name
3C-Medical Intelligence GmbH
Labeler DUNS
314546664
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-23
Public Version
5
Public Version Date
2023-12-15
Public Version Status
Update
Public Device Record Key
82ca3305-82b4-4ebb-9320-8bf17cfc8871

Device Description

BodyFIX® Manifold Cushion 500mm prevents the Cover Sheet from collapsing directly against the vacuum tube by distributing the airflow around the patient.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
40895 Vacuum-mould patient positioning system

Identifiers

Type ID
Primary 04056719001940

Premarket Submissions

Submission Number Supplement Number
K121530 000