FDA UDI In Commercial Distribution 🇺🇸 United States

Aculife

DI: 74719874910005 · Model: IDOC-01 Vitall · INNO HEALTH TECHNOLOGY CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
Aculife
Primary DI
74719874910005
Version / Model
IDOC-01 Vitall
Company Name
INNO HEALTH TECHNOLOGY CO., LTD.
Labeler DUNS
658605845
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2018-11-27
Public Version
1
Public Version Date
2018-12-28
Public Version Status
New
Public Device Record Key
0299f320-43d3-40e3-b303-a1f927c59171

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
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BWK Stimulator, Electro-Acupuncture

GMDN Terms

Code Name
34675 Acupuncture unit, home-use

Identifiers

Type ID
Primary 74719874910005
Unit of Use 04719874910006