TEMPO SRD6766

GUDID 20705032051177

5F TEMPO 0.038 INCHES 80CM C3

CORDIS CORPORATION

Angiographic catheter, single-use

• Primary Device ID: 20705032051177
• NIH Device Record Key: b6cde66d-b832-470c-9930-02a5a71615ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TEMPO
• Version Model Number: SRD6766
• Catalog Number: SRD6766
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Exposure to temperatures above 54 degrees C (130 F) may damage the catheter
• Special Storage Condition, Specify: Between 0 and 0 *To prevent damage to the catheter tip during removal from the package, grasp the hub and withdraw the catheter
• Special Storage Condition, Specify: Between 0 and 0 *Do not use if package is damanged
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dark, dry place
• Special Storage Condition, Specify: Between 0 and 0 *Exposure to temperatures above 54 degrees C (130 F) may damage the catheter
• Special Storage Condition, Specify: Between 0 and 0 *To prevent damage to the catheter tip during removal from the package, grasp the hub and withdraw the catheter
• Special Storage Condition, Specify: Between 0 and 0 *Do not use if package is damanged
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dark, dry place

Device Identifiers

Device Issuing Agency	Device ID
GS1	20705032051177 [Primary]

FDA Product Code

• DQO: CATHETER, INTRAVASCULAR, DIAGNOSTIC

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-01

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• 20705032064382: 4 F TEMPO 0.038 INCHES 80 CM SHK MOD
• 20705032064375: 4 F TEMPO 0.038 INCHES 80CM CONTRA I
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• 20705032051948: 4 F TEMPO 0.038 INCHES 80CM MPA1
• 20705032051795: 5 F TEMPO .038 INCHES 100CM VISCERAL
• 20705032051788: 5 F TEMPO .038 INCHES 100CM VISCERAL
• 20705032051771: 5 F TEMPO 0.038 INCHES 125CM VERT135
• 20705032051740: 4 F TEMPO 0.038 INCHES 40CM BER II
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• 20705032051597: 5 F TEMPO 0.035 INCHES 125CM 5SH PIG
• 20705032051573: 5 F TEMPO 0.035 INCHES 120CM J-CURVE
• 20705032051481: 5 F TEMPO 0.038 INCHES 100CM RC MOD.
• 20705032051436: 5 F TEMPO 0.038 INCHES 100CM SRC-2
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• 20705032051320: 5 F TEMPO 0.038 INCHES 100CM RH H2
• 20705032051191: 4 F TEMPO 0.038 INCHES 120 CM MANI
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• 20705032051108: 5F TEMPO 0.035 125CM 5SH STR
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