FDA UDI In Commercial Distribution 🇺🇸 United States

CHISEL

DI: 03596010470430 · Model: 7209648 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CHISEL
Primary DI
03596010470430
Version / Model
7209648
Catalog Number
7209648
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
3068dc80-f2d3-4453-bbaf-c9149c5c7631

Device Description

CHISEL VULCAN ANGLED

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
HRX ARTHROSCOPE

GMDN Terms

Code Name
10825 Orthopaedic chisel

Identifiers

Type ID
Primary 03596010470430

Customer Contacts