FDA UDI In Commercial Distribution 🇺🇸 United States

Coblation

DI: 00817470000696 · Model: AC2340-01 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Coblation
Primary DI
00817470000696
Version / Model
AC2340-01
Catalog Number
AC2340-01
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a35fc9e6-ecce-4451-b065-e5d0c71d2a0b

Device Description

2.7 MM INTEGRATED CABLE WAND ICW, SIDEWINDER BLADE 55 DEGREE

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

GMDN Terms

Code Name
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 00817470000696

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033584 000