FDA UDI In Commercial Distribution 🇺🇸 United States

K-3 AIRE ZONE

DI: 00817012030730 · Model: Pediatric Wave BB MS · KAP MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K-3 AIRE ZONE
Primary DI
00817012030730
Version / Model
Pediatric Wave BB MS
Catalog Number
Pediatric Wave BB MS
Company Name
KAP MEDICAL
Labeler DUNS
135241342
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-16
Public Version
1
Public Version Date
2022-12-26
Public Version Status
New
Public Device Record Key
e2accd09-546c-45ca-a85f-f44fe1908648

Device Description

Pediatric, Pulsating, Battery Backup, Mattress System, 60"x30"x6".

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
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
IOQ Bed, Flotation Therapy, Powered

GMDN Terms

Code Name
17593 Low-air-loss bed

Identifiers

Type ID
Primary 00817012030730

Customer Contacts

Phone
951-340-4360