FDA UDI In Commercial Distribution 🇺🇸 United States

WOK

DI: 00845699003631 · Model: 61600060 · WHEELCHAIRS OF KANSAS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WOK
Primary DI
00845699003631
Version / Model
61600060
Company Name
WHEELCHAIRS OF KANSAS
Labeler DUNS
063402450
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-13
Public Version
1
Public Version Date
2024-09-23
Public Version Status
New
Public Device Record Key
8c37412b-d8ba-46d1-a502-bafc8b0108fd

Device Description

230V Platinum 6000

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
FMR Device, Transfer, Patient, Manual

GMDN Terms

Code Name
36688 Alternating-pressure inflator

Identifiers

Type ID
Primary 00845699003631