FDA UDI In Commercial Distribution 🇺🇸 United States

ANSiSTIM - PP

DI: 08908006064267 · 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
08908006064267
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
f57e5011-6ba7-46c2-b493-e614c3f06eaf

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
NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief

GMDN Terms

Code Name
13763 Acupuncture electrical stimulation system

Identifiers

Type ID
Primary 08908006064267

Premarket Submissions

Submission Number Supplement Number
K220397 000