XI.D-RL™ XI.D-RL

GUDID 00885672009632

Disposable Extension Cable

Oscor Inc.

Electrical-only medical device connection cable, single-use
Primary Device ID00885672009632
NIH Device Record Keybf923d8e-d55e-4bcc-885d-965b0c35b89a
Commercial Distribution StatusIn Commercial Distribution
Brand NameXI.D-RL™
Version Model NumberXI.D-RL
Catalog NumberXI.D-RL
Company DUNS101835833
Company NameOscor Inc.
Device Count5
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(727)937-2511
Emailsales@oscor.com

Device Dimensions

Length250 Centimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100885672009632 [Unit of Use]
GS110885672009639 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IKDCABLE, ELECTRODE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-27
Device Publish Date2020-04-17

On-Brand Devices [XI.D-RL™]

04260451444013Disposable Extension Cable
00885672009632Disposable Extension Cable

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