FDA UDI In Commercial Distribution 🇺🇸 United States

Patient Kit, Synchrony

DI: 00852184003687 · Model: 20-3002 · Synapse Biomedical, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Patient Kit, Synchrony
Primary DI
00852184003687
Version / Model
20-3002
Company Name
Synapse Biomedical, Inc.
Labeler DUNS
138432070
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-23
Public Version
1
Public Version Date
2025-10-31
Public Version Status
New
Public Device Record Key
2bed3a89-8d71-4c24-bf0b-fd93919cd0d3

Device Description

Stimulator, Neuromuscular, External Functional

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
GZI Stimulator, Neuromuscular, External Functional
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00852184003687

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242704 000