FDA UDI In Commercial Distribution 🇺🇸 United States

WEREWOLF+

DI: 00885556804575 · Model: 72290177 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEREWOLF+
Primary DI
00885556804575
Version / Model
72290177
Catalog Number
72290177
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-01
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
277c5b1e-a31d-471e-af28-d98d02a8b255

Device Description

WEREWOLF + (RF20000-APL) POWER CORD/MANUAL- SCANDINAVIA

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
No
Has Lot/Batch Number
Yes
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 00885556804575

Customer Contacts