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Stryker Vertebral Bone Biopsy Kit - HSA Registration DE0008783

Access comprehensive regulatory information for Stryker Vertebral Bone Biopsy Kit in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0008783 and owned by Stryker Instruments. The device was registered on March 07, 2012.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS B
DE0008783
Stryker Vertebral Bone Biopsy Kit
HSA Registration Number: DE0008783
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Product Description

The Vertebral Bone Biopsy Kit is used with the ACM Percutaneous Delivery System and the PCD Precision System. The kit requires the use of a four-faceted tip introduction needle. The Bone Biopsy Kit is used to remove a sample of bone tissue for diagnostic purposes.

Device Classification
Device Class
CLASS B
Medical Speciality Area
General & Plastic Surgery
HSA Product Code
Refer to CRPNS
HS Code
90189090
Registration Information
Registration Number
DE0008783
Registration Date
March 07, 2012
Change Notification Approval Date
June 27, 2024
Retention Due Date
March 06, 2026
Product Owner
Short Name
Stryker Instruments
Address
1941 Stryker Way, Portage MI 49002, UNITED STATES
Registrant
Address
1 GEORGE STREET, ONE GEORGE STREET, #20-1/2/3, SINGAPORE 049145
Importer
Address
1 GEORGE STREET, ONE GEORGE STREET, #20-1/2/3, SINGAPORE 049145 5 JALAN KILANG BARAT, PETRO CENTRE, #09-00, SINGAPORE 159349
Model Information
Model Name(s)
10G Bone Biopsy Kit 11G Bone Biopsy Kit 13G Bone Biopsy Kit 9 Inch 10G Bone Biopsy Kit
Model Identifier(s)
306-105 306-115 306-135 306-195