FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03596010615503 · Model: 7210380 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03596010615503
Version / Model
7210380
Catalog Number
7210380
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
8
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
03eefeec-a468-4a15-8984-e6023092ea96

Device Description

ELECTROBLADE GENERATOR ADAPTER REQUIRED TO OPERATE 7205962, PACKAGED NON-STERILE, REUSABLE

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
HRX ARTHROSCOPE

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 03596010615503

Customer Contacts