DEVICE: Zoom RDL Radial Access System, 110cm (00812212030535)
Device Identifier (DI) Information
Zoom RDL Radial Access System, 110cm
ICTC088110R
In Commercial Distribution
ICTC088110R
IMPERATIVE CARE, INC.
ICTC088110R
In Commercial Distribution
ICTC088110R
IMPERATIVE CARE, INC.
Zoom RDL, 110cm with dilator
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
17846 | Vascular guide-catheter, single-use |
A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.
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Active | false |
10691 | Vascular microcatheter |
A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
DQY | Catheter, Percutaneous |
QJP | Catheter, Percutaneous, Neurovasculature |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K220807 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Special Storage Condition, Specify: Store in a cool, dry place at room temperature. |
Special Storage Condition, Specify: Avoid exposure to water, sunlight, extreme temperatures and high humidity during storage. |
Clinically Relevant Size
[?]Size Type Text |
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Lumen/Inner Diameter: 0.088 Inch |
Outer Diameter: 0.110 Inch |
Catheter Length: 110 Centimeter |
Device Record Status
e89d26c0-6262-45a3-a147-6bba1da4c9a6
February 06, 2025
2
September 28, 2022
February 06, 2025
2
September 28, 2022
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
1-408-502-7548
CustomerService@Imperativecare.com
CustomerService@Imperativecare.com