FDA UDI In Commercial Distribution 🇺🇸 United States

geko

DI: 05060294771609 · Model: W-3 · FIRSTKIND LTD
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
geko
Primary DI
05060294771609
Version / Model
W-3
Catalog Number
W3US01
Company Name
FIRSTKIND LTD
Labeler DUNS
216603021
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-14
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
88c3be8e-8a7f-404c-8325-0fee97ed88b0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 05060294771609
Package 05060294771616
Package 05060294771623

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K220327 000