FDA UDI In Commercial Distribution 🇺🇸 United States

ABLATOR

DI: 03596010470348 · Model: 7209658 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ABLATOR
Primary DI
03596010470348
Version / Model
7209658
Catalog Number
7209658
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
4
Public Version Date
2024-10-28
Public Version Status
Update
Public Device Record Key
17ebfc40-fdf8-41f4-a4dd-cae3c6b95f96

Device Description

PROBE ABLATOR 30 DEG

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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
HRX ARTHROSCOPE

GMDN Terms

Code Name
61875 Endoscopic electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Primary 03596010470348

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K003893 000