FDA UDI In Commercial Distribution 🇺🇸 United States

8013139

DI: 00816469021292 · Model: 8013139 · LASER PERIPHERALS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
8013139
Primary DI
00816469021292
Version / Model
8013139
Catalog Number
8013139
Company Name
LASER PERIPHERALS, LLC
Labeler DUNS
177234754
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-08
Public Version
2
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
b93b9a40-8f2b-412d-9832-95426b974920

Device Description

1000u Conical Tip Laser Fiber

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
47785 Urogenital surgical laser system beam guide, single-use

Identifiers

Type ID
Primary 00816469021292