FDA UDI In Commercial Distribution 🇺🇸 United States

COBLATION

DI: 00885556647462 · Model: 72290038 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COBLATION
Primary DI
00885556647462
Version / Model
72290038
Catalog Number
72290038
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-08
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
42db2d4c-fb2e-414a-aa04-6a114115bc81

Device Description

WEREWOLF FLOW 90 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
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 00885556647462

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183346 000