120260
Dura Mater Implants
硬膜植入物
Codman & Shurtleff, Inc.·IV·Hong Kong MDACS·Registered July 31, 2017Delisted
Device overview
- Risk class
- IV
- Product code
- 23846
- State
- N/A
- Status
- Delisted已退市
Manufacturer (製造商)
- Name
- Codman & Shurtleff, Inc.Codman & Shurtleff,Inc.
- Country
- United States美国
- Address
- 325 Paramount Drive, Raynham, Massachusetts, 02767-0350, USA美国马萨诸塞州雷因汉姆，帕拉蒙特大道325号，邮政编码：02767-0350
Authorised representative (AR)
- Name
- Johnson & Johnson (Hong Kong) Limited强生 (香港) 有限公司
- Phone
- 27386080
Regulatory timeline
- Registration date
- July 31, 2017
- Expiry date
- July 31, 2022
- Delist date
- March 25, 2019
Product models
Duraform Collagen Dural Graft Material (80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480)
Remarks
Delisted.
已從列表中刪除。
About this record
This profile provides complete Hong Kong MDACS registration information for Dura Mater Implants. Review device classification, authorised representative (AR) details, manufacturer contacts, product codes, and regulatory milestones. Pure Global AI delivers bilingual transparency for medical device registrations across Asia.
Product Info: Dura Mater Implants
產品資訊： 硬膜植入物