FDA UDI In Commercial Distribution 🇺🇸 United States

FiberLase™ HP-R 240 mm bent, curved tip

DI: 07290109141107 · Model: FiberLase™ HP-R 240 mm bent, curved tip · LUMENIS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FiberLase™ HP-R 240 mm bent, curved tip
Primary DI
07290109141107
Version / Model
FiberLase™ HP-R 240 mm bent, curved tip
Catalog Number
AC-1063980
Company Name
LUMENIS LTD.
Labeler DUNS
600166524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-25
Public Version
6
Public Version Date
2023-10-09
Public Version Status
Update
Public Device Record Key
edb0f579-d86f-41c9-8588-d4b711c6c042

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
61474 General/multiple surgical laser system beam guide, reusable

Identifiers

Type ID
Primary 07290109141107
Direct Marking 07290109143828

Customer Contacts

Phone
408-764-3000