FDA UDI In Commercial Distribution 🇺🇸 United States

Pentaflex

DI: 05056341676041 · Model: 250SL000/000 · Arjohuntleigh AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pentaflex
Primary DI
05056341676041
Version / Model
250SL000/000
Company Name
Arjohuntleigh AB
Labeler DUNS
355804758
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-30
Public Version
1
Public Version Date
2022-08-08
Public Version Status
New
Public Device Record Key
42e811bc-8fa2-492e-8980-4c49217a8f7a

Device Description

Pentaflex Replacement Mattress, 2 Way, 250kg,

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
IKY Mattress, Flotation Therapy, Non-Powered

GMDN Terms

Code Name
42328 Foam-filled bed mattress overlay

Identifiers

Type ID
Primary 05056341676041