GUDID 10814716020897

Fiber Optic Cable, Single-Use Disposable

COASTAL LIFE TECHNOLOGIES, INC.

Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use Urogenital surgical laser system beam guide, single-use
Primary Device ID10814716020897
NIH Device Record Key8bb67db3-2e48-4dcf-921d-079e2c8ce5d0
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberHMA-1060F
Company DUNS809254670
Company NameCOASTAL LIFE TECHNOLOGIES, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100814716020890 [Primary]
GS110814716020897 [Package]
Contains: 00814716020890
Package: [5 Units]
In Commercial Distribution

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-23

Devices Manufactured by COASTAL LIFE TECHNOLOGIES, INC.

10814716020224 - Surgimedics®2024-05-03 Smoke Evacuation Tubing
10814716020231 - Surgimedics®2024-05-03 Smoke Evacuation Tubing
10814716020262 - Surgimedics®2024-05-03 Smoke Evacuation Tubing Adapter
10814716020279 - Surgimedics®2024-05-03 Smoke Evacuation Tubing Adapter
10814716020729 - Surgimedics®2024-05-03 Smoke Evacuation Tubing Adapter
10814716020736 - Surgimedics®2024-05-03 Smoke Evacuation Tubing Adapter
10814716020743 - Surgimedics®2024-05-03 Smoke Evacuation Tubing Adapter
10814716020750 - Surgimedics®2024-05-03 Smoke Evacuation Tubing Adapter

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.