FDA UDI In Commercial Distribution 🇺🇸 United States

ProFoam Wedge 26x25x7

DI: 07640178060555 · Model: ProFoam Wedge 26x25x7 · Pearl Technology AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
ProFoam Wedge 26x25x7
Primary DI
07640178060555
Version / Model
ProFoam Wedge 26x25x7
Catalog Number
1152
Company Name
Pearl Technology AG
Labeler DUNS
480151859
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-11
Public Version
1
Public Version Date
2022-05-19
Public Version Status
New
Public Device Record Key
0b508dd2-802a-4a23-a2fd-1f9b3788fd41

Device Description

Universal patient positioning aid for MR and CT imaging.

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 07640178060555

Customer Contacts

Phone
+41435350840