FDA UDI In Commercial Distribution 🇺🇸 United States

SCULPTOR

DI: 03596010505170 · Model: 7210695 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCULPTOR
Primary DI
03596010505170
Version / Model
7210695
Catalog Number
7210695
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
40d7379d-ff12-4f8b-a5b7-f4bbfcc9e7ce

Device Description

VULCAN SCULPTOR-S 90DEG HP 3.0MM

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
HRX ARTHROSCOPE
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
61869 Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 03596010505170

Customer Contacts