FDA UDI In Commercial Distribution 🇺🇸 United States

SMK™

DI: 05415067028778 · Model: SMK-S1005-20 · ST. JUDE MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SMK™
Primary DI
05415067028778
Version / Model
SMK-S1005-20
Catalog Number
SMK-S1005-20
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-10
Public Version
9
Public Version Date
2023-10-06
Public Version Status
Update
Public Device Record Key
d0facce0-9126-42c1-9f2e-eb386ad879b8

Device Description

Radiofrequency Cannula - Straight

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXI PROBE, RADIOFREQUENCY LESION
GXD Generator, lesion, radiofrequency

GMDN Terms

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

Identifiers

Type ID
Primary 05415067028778
Package 15415067028775

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10 Centimeter
Needle Gauge 20 Gauge

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool and dry place; avoid exposure to extreme temperatures