FDA UDI In Commercial Distribution 🇺🇸 United States

MYO

DI: 05056701110147 · Model: BT KINISI 7 3/4 RH EU WRIST · HUGH STEEPER LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MYO
Primary DI
05056701110147
Version / Model
BT KINISI 7 3/4 RH EU WRIST
Catalog Number
KIN775REU-BT
Company Name
HUGH STEEPER LIMITED
Labeler DUNS
210280350
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-06
Public Version
1
Public Version Date
2023-07-14
Public Version Status
New
Public Device Record Key
76d26f66-a662-4602-b7a9-beb6f36a34e6

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
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
IQZ Hand, External Limb Component, Powered

GMDN Terms

Code Name
41497 Myoelectric hand prosthesis

Identifiers

Type ID
Primary 05056701110147