Medcxy

产品档案由注册证、说明书原文与平台整理数据生成

乔雅登Juvéderm

就这个产品提问

乔雅登是一款玻尿酸填充产品，注册人 Allergan。库里关联的注册证：美国 P110033、美国 P050047。美国首次批准于 2013-10-22（P110033）。数据截至 2026-11-09。

  • 监管属性玻尿酸填充 · 监管属性未定
  • 注册人Allergan
  • 辖区US
  • 档案更新于2026-11-09 · v1

注册与基本资料公开可看；交叉发现与价格需要登录

注册与基本资料

乔雅登

产品
监管属性
未定（还没有核实过的注册证关联）未能核实
品类
玻尿酸填充
美国 · FDA PMA
P110033（关联待人工确认）
美国 · FDA PMA
P050047（关联待人工确认）
证上名称
JUVEDERM VOLUMA XC
注册人
Allergan
首次批准
2013-10-22
官网核对
还没有与官网现页逐字段核对

公开信息：注册证原文字段。注册人与日期取自 P110033；共关联 2 张证。这个产品实体还在待人工确认。

说明书对照（分辖区）

同一属性在不同辖区说明书里的原文；没写的标「原文未报告」，不适用的标「不适用」

暂无数据

注册时间线

  1. US

    P050047 首次批准

  2. US

    P110033 首次批准

  3. US

    P050047 · P050047/S102

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜approval for an additional quality control step during the manufact…

  4. US

    P050047 · P050047/S103

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜undefined

  5. US

    P110033 · P110033/S085

    Normal 180 Day Track｜Change Design/Components/Specifications/Material｜for changes to optimize the Juvederm manufacturing processes.

  6. US

    P110033 · P110033/S100

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜a change in location for manufacturing the tip cap component

  7. US

    P050047 · P050047/S104

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜a change in location for manufacturing the tip cap component

  8. US

    P110033 · P110033/S101

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜to update the varnish used in the manufacture of Juvederm carton bo…

  9. US

    P050047 · P050047/S105

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜to update the varnish used in the manufacture of Juvederm carton bo…

  10. US

    P110033 · P110033/S099

    Panel Track｜Labeling Change - Indications/instructions/shelf life/tradename｜SKINVIVE by JUVÉDERM® is indicated for intradermal injection to …

  11. US

    P110033 · P110033/S091

    Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval for using the sodium hyaluronate manufactured from HTL’s addi…

  12. US

    P050047 · P050047/S098

    Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval for using the sodium hyaluronate manufactured from HTL’s addi…

  13. US

    P110033 · P110033/S102

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approval for an automated Manufacturing Execution System used for t…

  14. US

    P050047 · P050047/S107

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approval for an automated Manufacturing Execution System used for t…

分开写首次批准、本证核发（延续或变更后会更新）、变更与有效期；首次批准为空表示未从官方来源取到。每张证只列最近 6 条变更，完整记录点编号看注册证原文。海外证的日期照原文的叫法：英国器械是登记日期（MHRA 不审批），澳大利亚是列入 ARTG 的日期，FDA 器械是决定日期。

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最近变化

5
  • P110033：30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approva…2026-08-28
  • P050047：30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approva…2026-08-28
  • P110033：Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval f…2026-08-11
  • P050047：Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval f…2026-08-11
  • P110033：Panel Track｜Labeling Change - Indications/instructions/shelf life/tradename｜SKIN…2026-06-11

资料

2