Morrison Steerable Needle 13550

GUDID 27350031355509

Morrison Steerable Needle 21G 17cm. Percutaneous injection and aspiration procedures and tissue sampling in liver, kidney, muscle and subcutaneous tissue.

Apriomed AB

Body aspiration needle, single-use

• Primary Device ID: 27350031355509
• NIH Device Record Key: b11e47c7-6a39-4be9-96ca-010fe03fac88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Morrison Steerable Needle
• Version Model Number: 13550
• Catalog Number: 13550
• Company DUNS: 631734758
• Company Name: Apriomed AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Customer Support Contacts

• Phone: +46184301440
• Email: info@apriomed.com

Device Dimensions

• Needle Gauge: 21 Gauge
• Needle Gauge: 21 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350031355505 [Primary]
GS1	17250031355502 [Package]; Contains: 07350031355505; Package: Shelf box [10 Units]; In Commercial Distribution
GS1	17350031355502 [Package]; Contains: 07350031355505; Package: Shelf box [10 Units]; In Commercial Distribution
GS1	27350031355509 [Package]; Contains: 17350031355502; Package: Transportation box [18 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150625

FDA Product Code

• KNW: Instrument, Biopsy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-06-27
• Device Publish Date: 2016-09-05

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• 17350031350286 - Bonopty Penetration Set: 2023-05-02 Manually operated, sterile, single use coaxial bone biopsy system.
• 17350031350293 - Bonopty Biopsy Set: 2023-05-02 Manually operated, sterile, single use coaxial bone biopsy system.
• 17350031350309 - Bonopty Penetration Set: 2023-05-02 Manually operated, sterile, single use coaxial bone biopsy system.