FDA UDI In Commercial Distribution 🇺🇸 United States

WEREWOLF

DI: 00885556775592 · Model: 72290144S · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEREWOLF
Primary DI
00885556775592
Version / Model
72290144S
Catalog Number
72290144S
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-17
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
dd22b016-0e2f-443a-ba74-37a0765ab8e8

Device Description

ENT RF20000 CONTROLLER REFURBISHED

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 00885556775592

Customer Contacts