FDA UDI Not in Commercial Distribution 🇺🇸 United States

Coblation

DI: 00817470004274 · Model: KC8000-00 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Coblation
Primary DI
00817470004274
Version / Model
KC8000-00
Catalog Number
KC8000-00
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
18af62f6-ce14-4124-b82b-24d132a29048
Distribution End Date
2022-03-17

Device Description

SYSTEM 2000 CONTROLLER (120V)

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
11490 Electrosurgical system generator

Identifiers

Type ID
Primary 00817470004274

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K011634 000