FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 06959664925140 · Model: AG-5302-242523 · Hangzhou AGS MedTech Co., Ltd.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
06959664925140
Version / Model
AG-5302-242523
Company Name
Hangzhou AGS MedTech Co., Ltd.
Labeler DUNS
542984702
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-15
Public Version
1
Public Version Date
2026-04-23
Public Version Status
New
Public Device Record Key
87238f49-bf8e-455e-848b-28f2c65ea26b

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

GMDN Terms

Code Name
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Package 16959664925147
Primary 06959664925140
Package 26959664925144

Premarket Submissions

Submission Number Supplement Number
K192342 000