GUDID 00763000747480

CATHETER C320LBBS48 SMALL CURVE 48 GBL

MEDTRONIC, INC.

Vascular guide-catheter, single-use
Primary Device ID00763000747480
NIH Device Record Key0503e38b-3379-4847-bdb7-48ee65fb0223
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberC320LBBS48
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 Usetrue
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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Device Size Text, specify0
Catheter Working Length48 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Catheter Working Length48 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Catheter Working Length48 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Catheter Working Length48 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Catheter Working Length48 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000747480 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQYCatheter, percutaneous

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-17
Device Publish Date2026-02-09

Devices Manufactured by MEDTRONIC, INC.

00763000747459 - NA2026-02-17 CATHETER C320LBBL45 LARGE CURVE 45 GBL
00763000747466 - NA2026-02-17 CATHETER C320LBBL48 LARGE CURVE 48 GBL
00763000747473 - NA2026-02-17 CATHETER C320LBBS45 SMALL CURVE 45 GBL
00763000747480 - NA2026-02-17CATHETER C320LBBS48 SMALL CURVE 48 GBL
00763000747480 - NA2026-02-17 CATHETER C320LBBS48 SMALL CURVE 48 GBL
00199150006045 - N/A2026-02-10 COMM HANDSET KIT TH90D01 DBS EMANUAL US
00199150068302 - NA2026-02-10 CUSTOM PACK BB12M12R7 HLO CPB
20199150068351 - NA2026-02-10 CUSTOM PACK 12C75R1 20PK ACC BIDMC-PCK
20199150068382 - NA2026-02-10 CUSTOM PACK BB12C41R9 10PK ACC LNG PK

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