FDA UDI In Commercial Distribution 🇺🇸 United States

ANSiSTIM-PP

DI: 08908006064281 · Model: ANSiSTIM-PP · DYANSYS INDIA PRIVATE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANSiSTIM-PP
Primary DI
08908006064281
Version / Model
ANSiSTIM-PP
Company Name
DYANSYS INDIA PRIVATE LIMITED
Labeler DUNS
916731981
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-16
Public Version
1
Public Version Date
2026-03-24
Public Version Status
New
Public Device Record Key
18bf74de-6ba7-4203-a90d-ad39f09ff087

Device Description

ANSiSTIM-PP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BWK Stimulator, Electro-Acupuncture

GMDN Terms

Code Name
13763 Acupuncture electrical stimulation system

Identifiers

Type ID
Primary 08908006064281