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FeimanMedical Collagen Filler

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Feiman is a Collagen product (Class III device), registered by 斐缦（长春）医药生物科技有限责任公司. Linked registrations: China 国械注准20163131609. Data as of 2026-10-24.

  • Regulatory classCollagen · Class III device
  • Holder斐缦（长春）医药生物科技有限责任公司
  • JurisdictionsCN
  • Updated2026-10-24 · v1

Registration and basics are public; findings and prices need an account

Registration and basics

Feiman

Product
Regulatory class
Class III device
Category
Collagen
China · NMPA device registration
国械注准20163131609
Name on registration
医用胶原充填剂
Registrant
斐缦（长春）医药生物科技有限责任公司
First approval
Not obtained from an official source
This certificate issued
2021-11-03
Valid until
2026-11-02
Models and sizes
1ml；0.5ml
Checked against official page
2026-10-24

Public: fields from the registration record.

Label facts by jurisdiction

What each jurisdiction's label says for the same attribute; gaps are marked Not reported, irrelevant ones N/A

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Registration timeline

  1. CN

    国械注准20163131609 this certificate issued

    Issue date of this certificate, not the first approval

  2. CN

    国械注准20163131609 change

    官网变更：注册人住所由长春净月高新技术产业开发区南环城路与和融路交汇证大立方大厦1号楼1609-76;变更为：长春市净月开发区新城大街6645号。

  3. CN

    国械注准20163131609 change

    官网变更：生产地址由长春高新区光谷大街1050号;变更为：长春高新区光谷大街1050号；长春市净月开发区新城大街6645号（2～8℃冷库）。

  4. CN

    国械注准20163131609 change

    官网变更：生产地址由长春高新区光谷大街1050号；长春市净月开发区新城大街6645号（2~8℃冷库）;变更为：长春高新区光谷大街1050号，长春市净月开发区新城大街6645号。

  5. CN

    国械注准20163131609 change

    延续或变更注册获批（受理号 CQX2501099；2026年05月08日医疗器械批准证明文件送达信息）

  6. CN

    国械注准20163131609 change

    官网变更：一、 型号规格变更内容见附件。二、 结构及组成变更内容见附件。三、 产品技术要求变更内容见附件。

  7. CN

    国械注准20163131609 change

    延续或变更注册获批（受理号 CQY2600640；2026年06月09日医疗器械批准证明文件送达信息）

  8. CN

    国械注准20163131609 valid until

First approval, this certificate's issue date (updated after renewals or changes), changes and expiry are listed separately; a missing first approval means it was not obtained from an official source. Up to 6 recent changes per registration; click the number for the full record.

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Recent changes

5
  • 国械注准20163131609: 延续或变更注册获批（受理号 CQY2600640；2026年06月09日医疗器械批准证明文件送达信息）2026-06-03
  • 国械注准20163131609: 延续或变更注册获批（受理号 CQX2501099；2026年05月08日医疗器械批准证明文件送达信息）2026-04-30
  • 国械注准20163131609: 官网变更：一、 型号规格变更内容见附件。二、 结构及组成变更内容见附件。三、 产品技术要求变更内容见附件。2026-04-30
  • 国械注准20163131609: 官网变更：生产地址由长春高新区光谷大街1050号；长春市净月开发区新城大街6645号（2~8℃冷库）;变更为：长春高新区光谷大街1050号，长春市净月开发区新城…2025-01-21
  • 国械注准20163131609: 官网变更：生产地址由长春高新区光谷大街1050号;变更为：长春高新区光谷大街1050号；长春市净月开发区新城大街6645号（2～8℃冷库）。2024-11-06

Sources

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