FDA UDI In Commercial Distribution 🇺🇸 United States

Epimed

DI: 00818788023667 · Model: 282-1615 · EPIMED INTERNATIONAL, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Epimed
Primary DI
00818788023667
Version / Model
282-1615
Company Name
EPIMED INTERNATIONAL, INC
Labeler DUNS
799751953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-04
Public Version
2
Public Version Date
2025-11-24
Public Version Status
Update
Public Device Record Key
72065a70-f1c9-4dd9-ac74-5c16b7c3f91c

Device Description

R-F™ Cannula B Bevel 16g TW x 15cm w/ 10mm Active Tip

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
MR Unsafe
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
GXI Probe, radiofrequency lesion

GMDN Terms

Code Name
58739 Percutaneous radio-frequency ablation probe cannula, single-use

Identifiers

Type ID
Package 10818788023664
Primary 00818788023667

Premarket Submissions

Submission Number Supplement Number
K041021 000

Device Sizes

Type Value Unit Text
Length 15 Centimeter
Length 10 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit