FDA UDI Not in Commercial Distribution 🇺🇸 United States

Novus Spectra

DI: 07290109143248 · Model: Novus Spectra · LUMENIS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Novus Spectra
Primary DI
07290109143248
Version / Model
Novus Spectra
Company Name
LUMENIS INC.
Labeler DUNS
043618763
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-24
Public Version
5
Public Version Date
2024-01-17
Public Version Status
Update
Public Device Record Key
7f142c3e-5bea-4a86-932f-1c65a90ab21c
Distribution End Date
2024-01-15

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
36150 General/multiple surgical frequency-doubled solid-state laser system

Identifiers

Type ID
Primary 07290109143248

Customer Contacts

Phone
408-764-3000