PDO Max Cannulas CAN21100

GUDID 00850018324472

Cannula, Surgical, General and Plastic Surgery

Max Pdo Inc

Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use

• Primary Device ID: 00850018324472
• NIH Device Record Key: be063316-97c5-4bbc-acf1-89f8513642cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PDO Max Cannulas
• Version Model Number: CAN21100
• Catalog Number: CAN21100
• Company DUNS: 043570058
• Company Name: Max Pdo Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850018324472 [Primary]

FDA Product Code

• GEA: Cannula, Surgical, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-01
• Device Publish Date: 2021-03-24

Devices Manufactured by Max Pdo Inc

• 00850018324656 - PDO Max Threads: 2022-07-28 Duo 420mm Sterile Inner
• 00850018324663 - PDO Max Threads: 2022-07-28 Duo Molded 420mm Sterile Inner
• 00850018324670 - PDO Max Threads: 2022-07-28 Duo Molded 420mm - Foil Pack
• 00850018324687 - PDO Max Threads: 2022-07-28 Duo 420mm - Foil Pack Copy
• 00850018324625 - PDO Max Threads: 2022-06-16 Levo Lock 18gx100mm Sterile Inner
• 00850018324632 - PDO Max Threads: 2022-06-16 Levo Lock 18gx100mm Foil Pack
• 00850018324601 - PDO Max Threads: 2021-10-12 Double Ciclone 25gx38mm Sterile Inner
• 00850018324618 - PDO Max Threads: 2021-10-12 Double Ciclone 25gx38mm Foil Pack