FDA UDI In Commercial Distribution 🇺🇸 United States

Lumax

DI: 60888937013452 · Model: 53366 · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lumax
Primary DI
60888937013452
Version / Model
53366
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
5
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
3cb3046a-c1d0-41ac-9ba0-f6b7598d89eb

Device Description

Lumax™ TS Pro • EMG Software Upgrade Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
FEN Device, Cystometric, Hydraulic

GMDN Terms

Code Name
14307 Urodynamic measurement system

Identifiers

Type ID
Primary 60888937013452

Premarket Submissions

Submission Number Supplement Number
K953734 000