FDA UDI In Commercial Distribution 🇺🇸 United States

K-0SG SkinGuard

DI: 00817012023381 · Model: K-0SG · KAP MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K-0SG SkinGuard
Primary DI
00817012023381
Version / Model
K-0SG
Catalog Number
K-0SG
Company Name
KAP MEDICAL
Labeler DUNS
135241342
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-03
Public Version
1
Public Version Date
2020-04-13
Public Version Status
New
Public Device Record Key
3d33a765-cbca-4fcd-a30b-07df3c3089c4

Device Description

K-0SG SkinGuard Micorclimate Control Unit

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 00817012023381

Customer Contacts

Phone
951-340-4360