FDA UDI In Commercial Distribution 🇺🇸 United States

COBLATION

DI: 00885556617472 · Model: 72290037 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COBLATION
Primary DI
00885556617472
Version / Model
72290037
Catalog Number
72290037
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-24
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a5b099a4-4061-4439-9ec7-f40fa7aef27f

Device Description

WEREWOLF FLOW 50 COBLATION WAND

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
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 00885556617472

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143235 000
K162074 000