FDA UDI In Commercial Distribution 🇺🇸 United States

RFTL

DI: 14048223016777 · Model: 011165-30D · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
RFTL
Primary DI
14048223016777
Version / Model
011165-30D
Catalog Number
011165-30D
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-01
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
f2004354-8984-4bd5-ad06-b209fe2b5510
Distribution End Date
2025-03-15

Device Description

RFTL curved 20G x 98,6mm stimulation tip 10mm, grinding 15°

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
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
No

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 14048223016777
Unit of Use 04048223016770

Customer Contacts