PMDA device listing
ミュータスワコー AFP-L3・i50(2、2022年2月作成（第1版）)
PMDA In vitro diagnostic listing · 23000EZX00013000 · Class III
Key facts
| PMDA document key | 890027_23000EZX00013000_B_01 |
|---|---|
| Brand names | ミュータスワコー AFP-L3・i50(2、2022年2月作成（第1版）) |
| General names (JMDN) | アルファーフェトプロテインのレクチン反応性による分画比キット |
| Product type | In vitro diagnostic |
| Device class (Japan) | Class III |
| Approval, certification or notification number | 23000EZX00013000 |
| JMDN codes | 43480000 |
| Category code | A0100 |
| Marketing authorization holder | 製造販売／富士フイルム和光純薬株式会社 |
| Package insert date | Feb 13, 2022 |
| Latest revision | 2022-02 |
| PMDA product page | pmda.go.jp |
| Package insert on pmda.go.jp | pmda.go.jp |
At a glance
- 1–9 Package insert revisions
- None Related PMDA documents
- Listed Listed on the PMDA site
- No Refers to a technical manual
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA medical device and IVD listings (Japan)
Medical devices and in vitro diagnostics sold in Japan are approved by the MHLW, certified by a registered certification body or notified, depending on class, and the PMDA publishes each product's package insert. Only identifiers, names and dates are shown here; package insert text and review reports are not reproduced.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan, medical device package insert database · Source date: