FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03596010479587 · Model: 7205902 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03596010479587
Version / Model
7205902
Catalog Number
7205902
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-23
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
da60bc5c-cc46-4c92-948d-6434847fa593

Device Description

MTO REPLACEMENT(THREAD ON)SOAK CAP

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
45804 Electrical mains power cable

Identifiers

Type ID
Primary 03596010479587

Customer Contacts