FDA UDI In Commercial Distribution 🇺🇸 United States

LENS

DI: 00885556631980 · Model: 72203967S · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LENS
Primary DI
00885556631980
Version / Model
72203967S
Catalog Number
72203967S
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-15
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
3e77fc13-23cf-4ffc-8f59-1d4254688b68

Device Description

SERVICE REPLACEMENT CAMERA HEAD LENS INTEGRATED SYSTEM

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
Liquid Chemical

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery
HRX Arthroscope

GMDN Terms

Code Name
35616 Endoscopic video imaging system

Identifiers

Type ID
Primary 00885556631980

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K153606 000