Primary Device ID | 00816469021612 |
NIH Device Record Key | 0d9fe087-b986-45b7-8954-d0eb9cab710b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DB-600R-5 |
Version Model Number | DB-600R-5 |
Catalog Number | DB-600R-5 |
Company DUNS | 177234754 |
Company Name | LASER PERIPHERALS, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816469021612 [Primary] |
GEX | Powered laser surgical instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-29 |
Device Publish Date | 2021-11-19 |
00816469021629 - DBSS-272 | 2022-05-30 272u Laser Fiber |
00816469021636 - DBSS-272-PL | 2022-05-30 272u Laser Fiber PL |
00816469021612 - DB-600R-5 | 2021-11-29600u Reduced Buffer Laser Fiber 5 use |
00816469021612 - DB-600R-5 | 2021-11-29 600u Reduced Buffer Laser Fiber 5 use |
00816469021599 - HTB-800 | 2021-03-30 800u Laser Fiber |
00816469021605 - HTB-800-PL | 2021-03-30 800u Laser Fiber PL |
00816469021582 - DB-600R-HPT-PL | 2020-09-29 600u Reduced Buffer Laser Fiber w/ HPT PL |
00816469021537 - LG-272-N-PL-M | 2020-08-18 LaseGuide® Nav 272u Laser Fiber PL |
00816469021544 - LG-365-E-PL-M | 2020-08-18 LaseGuide® Edge 365u Laser Fiber PL |