FDA UDI In Commercial Distribution 🇺🇸 United States

DYONICS ELECTROBLADE BONECUTTER

DI: 00885554015348 · Model: 72202213 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DYONICS ELECTROBLADE BONECUTTER
Primary DI
00885554015348
Version / Model
72202213
Catalog Number
72202213
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
d6ae05db-5488-4d53-8031-a8af1418c318

Device Description

4.5 MM DYONICS BONECUTTER ELECTROBLADE, YELLOW, PACKAGED 3 PER BOX, STERILE

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
56296 Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Package 20885554015342
Primary 00885554015348

Customer Contacts