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一次性使用内窥镜手术抓钳 - NMPA Registration 京械注准20242020716

Access comprehensive regulatory information for 一次性使用内窥镜手术抓钳 in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 京械注准20242020716 and owned by B.J.Zh.F.Panther Medical Equipment Co., Ltd.. The device was approved on November 26, 2024.

This page provides complete registration details including registrant information, province location (Beijing), intended use, and regulatory compliance data from the official China NMPA medical device database. Pure Global AI offers free access to China's complete medical device registry, helping global MedTech companies navigate NMPA regulations efficiently.

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Class II
京械注准20242020716
一次性使用内窥镜手术抓钳
NMPA Registration Number: 京械注准20242020716
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Pricing
Intended Use
English

与内窥镜配合使用,在内窥镜手术中穿过软组织达到人体解剖学上的指定区域,对目标组织进行抓取、夹持和处理软组织.

中文

与内窥镜配合使用，在内窥镜手术中穿过软组织达到人体解剖学上的指定区域，对目标组织进行抓取、夹持和处理软组织。

Device Classification
Device Class
Class II
Approval Department
Beijing Municipal Drug Administration
北京市药品监督管理局
Registration Information
Registration Number
京械注准20242020716
Approval Date
November 26, 2024
Expiry Date
November 25, 2029
Registrant
Name
B.J.Zh.F.Panther Medical Equipment Co., Ltd.
北京派尔特医疗科技股份有限公司
Province/Region
Beijing
北京
Address
The third floor of Building 1, No. 28 Torch Street, Science and Technology Park, Changping District, Beijing
北京市昌平区科技园区火炬街28号1号楼三层
Production Facility
Production Address
北京市昌平区北七家镇亚市南路C8号;北京市昌平区北七家镇上承路8
Storage Conditions and Expiration
English

5

Additional Information
Changes
生产地址变更为：北京市昌平区北七家镇亚市南路C8号;北京市昌平区北七家镇上承路8。规格变更为：见附页。产品过期日期变更为：5。
Appendix
产品技术要求