FDA UDI In Commercial Distribution 🇺🇸 United States

Epimed

DI: 00818788021786 · Model: 261-2010 · EPIMED INTERNATIONAL, INC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Epimed
Primary DI
00818788021786
Version / Model
261-2010
Catalog Number
261-2010
Company Name
EPIMED INTERNATIONAL, INC
Labeler DUNS
799751953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-24
Public Version
7
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
5675c9df-d641-4fb3-82c4-9a617e4fc503

Device Description

R-F™ Cannula Blunt 20g TW x 10cm w/ 5mm 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
Yes
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
Primary 00818788021786
Package 20818788021780
Package 10818788021783

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K041021 000

Device Sizes

Type Value Unit Text
Length 5 Millimeter
Length 10 Centimeter
Needle Gauge 20 Gauge
Device Size Text, specify 20g
Device Size Text, specify 5mm Active Tip
Device Size Text, specify 10 cm

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit