FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 06959664913871 · Model: AG-5461-0516 · Hangzhou AGS MedTech Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
06959664913871
Version / Model
AG-5461-0516
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
1a801fe0-11d2-4f92-8445-09c41503ac66

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
KGE Forceps, Biopsy, Electric

GMDN Terms

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

Identifiers

Type ID
Package 16959664913878
Primary 06959664913871
Package 26959664913875

Premarket Submissions

Submission Number Supplement Number
K210406 000