FDA UDI In Commercial Distribution 🇺🇸 United States

JRF-Pad-01

DI: 08800020102836 · Model: JRF-Pad-01 · Jeisys Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
JRF-Pad-01
Primary DI
08800020102836
Version / Model
JRF-Pad-01
Company Name
Jeisys Medical Inc.
Labeler DUNS
690275362
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2025-12-10
Public Version
1
Public Version Date
2025-12-18
Public Version Status
New
Public Device Record Key
90599b90-fe80-490a-9712-25936bbf758b

Device Description

JRF-Pad-01

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 08800020102836
Unit of Use 08800020106810

Premarket Submissions

Submission Number Supplement Number
K183284 000