FDA UDI Not in Commercial Distribution 🇺🇸 United States

Acculite EndoOcular

DI: 07290109140780 · Model: Illum/Sm Plug, 20ga str, SMA 906, 200µm · LUMENIS INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Acculite EndoOcular
Primary DI
07290109140780
Version / Model
Illum/Sm Plug, 20ga str, SMA 906, 200µm
Company Name
LUMENIS INC.
Labeler DUNS
043618763
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-25
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
81d0a691-4b33-41a8-b828-18baacd8ce68
Distribution End Date
2020-02-21

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
HQF Laser, Ophthalmic

GMDN Terms

Code Name
61162 Ophthalmic laser system beam guide

Identifiers

Type ID
Package 17290109140787
Primary 07290109140780

Customer Contacts

Phone
408-764-3000