GUDID 00643169315747

SYSTEM ACS500 AUTOCLAMP KIT NON RoHS

MEDTRONIC, INC.

Medical tubing clip/clamp, non-calibrated, reusable Medical tubing clip/clamp, non-calibrated, reusable
Primary Device ID00643169315747
NIH Device Record Keyc72e16dc-43ce-4d30-8364-3cc213ec3f1b
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberACS500
Company DUNS006261481
Company NameMEDTRONIC, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Operating and Storage Conditions

Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169315747 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWAControl, pump speed, cardiopulmonary bypass

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-05
Device Publish Date2018-11-04

Devices Manufactured by MEDTRONIC, INC.

00763000951825 - NA2024-05-31 CUSTOM PACK SSBB12G88R STERILE SMPL
00763000953423 - NA2024-05-31 CUSTOM PACK BB12F51R2 E ASSIST PACK
00763000953614 - NA2024-05-31 CUSTOM PACK HY0A20R46 CHRST NN
00763000953621 - NA2024-05-31 CUSTOM PACK BB11Q49R11 3/8 EC
00763000953638 - NA2024-05-31 CUSTOM PACK BB12A45R1 SMALL LOOP
00763000953645 - NA2024-05-31 CUSTOM PACK BB12A44R2 LRG AV LOOP
20763000953663 - NA2024-05-31 CUSTOM PACK BB12G60R 2PK 2PK CHRST TBL
00763000953676 - NA2024-05-31 CUSTOM PACK BB7B00R26 UW CMAG PK
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.