FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00885554024166 · Model: 72202962 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885554024166
Version / Model
72202962
Catalog Number
72202962
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
7
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
5125bd2b-2d06-42d7-a41e-3c71d33559e6

Device Description

VIDEOARTHROSCOPE NON-AUTOCLAVABLE, BLACK FOCUS RING, 19.5 MM FOCAL LENGTH, 4.0 MM OUTER DIAMETER X 70 DEGREE DIRECTION OF VIEW, 115 DEGREE FIELD OF VIEW,

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Hydrogen Peroxide

Product Codes

Code Name
EOB NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)
HRX ARTHROSCOPE

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 00885554024166

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K043395 000