FDA UDI In Commercial Distribution 🇺🇸 United States

FiberLase™ Endoscope Protection Sheath

DI: 07290109142036 · Model: FiberLase™ Endoscope Protection Sheath · LUMENIS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FiberLase™ Endoscope Protection Sheath
Primary DI
07290109142036
Version / Model
FiberLase™ Endoscope Protection Sheath
Company Name
LUMENIS LTD.
Labeler DUNS
600166524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-30
Public Version
4
Public Version Date
2021-10-21
Public Version Status
Update
Public Device Record Key
1afa8953-f807-4299-a946-21ea103e872e

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
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
17774 General/multiple surgical solid-state/carbon dioxide laser system

Identifiers

Type ID
Package 17290109142033
Primary 07290109142036

Customer Contacts

Phone
408-764-3000