FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00885554018783 · Model: 72202959 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885554018783
Version / Model
72202959
Catalog Number
72202959
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
9dedb1e7-5958-497d-a9bc-4e70d81cd4f6

Device Description

VIDEOARTHROSCOPES, AUTOCLAVABLE, HIGH DEFINITION 560H ONLY, 4.0 MM OUTER DIAMETER, 30 DEGREE DIRECTION OF VIEW, 115 DEGREE FIELD OF VIEW, 160 MM WORKING LENGTH, J-LOCK

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
HRX ARTHROSCOPE
EOB NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 00885554018783

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K043395 000