FDA UDI In Commercial Distribution 🇺🇸 United States

ProBelt

DI: 07640178061897 · Model: ProBelt 200 R3 H · Pearl Technology AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ProBelt
Primary DI
07640178061897
Version / Model
ProBelt 200 R3 H
Catalog Number
1286
Company Name
Pearl Technology AG
Labeler DUNS
480151859
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-17
Public Version
1
Public Version Date
2025-12-25
Public Version Status
New
Public Device Record Key
c972d102-40b9-4c81-9d90-79f017aa334e

Device Description

Short-term patient positioning and stabilization device during invasive and non-invasive procedures to be used on intact patient’s skin. Non-Sterile and not to be used in the sterile field.

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
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXH Cradle, Patient, Radiologic

GMDN Terms

Code Name
61131 Radiological general body-part positioner

Identifiers

Type ID
Primary 07640178061897