Angios Classic Angiographic Catheter Kit ANG3-0242

GUDID 00836559008248

Angiographic Catheter Kit, 6F

Oscor Inc.

Angiographic catheter, single-use
Primary Device ID00836559008248
NIH Device Record Keya2da14cd-9ceb-4a54-a246-768b574edb0a
Commercial Distribution StatusIn Commercial Distribution
Brand NameAngios Classic Angiographic Catheter Kit
Version Model NumberANG3-0242
Catalog NumberANG3-0242
Company DUNS101835833
Company NameOscor Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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

Device Size Text, specify0

Operating and Storage Conditions

Storage Environment TemperatureBetween 5 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100836559008248 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-11-16

On-Brand Devices [Angios Classic Angiographic Catheter Kit]

00836559008248Angiographic Catheter Kit, 6F
00836559008231Angiographic Catheter Kit, 6F
00836559008125Angiographic Catheter Kit, 6F
00836559008118Angiographic Catheter Kit, 6F
00836559007944Angiographic Catheter Kit, 5F
00836559007937Angiographic Catheter Kit, 5F
00836559007821Angiographic Catheter Kit, 5F
00836559007814Angiographic Catheter Kit, 5F

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