PMDA device listing
ケー・エックス３
PMDA Medical device listing · 226AABZX00049000 · Class II
Key facts
| PMDA document key | 100113_226AABZX00049000_A_02 |
|---|---|
| Brand names | ケー・エックス３ |
| General names (JMDN) | ポータブルアナログ式汎用一体型X線診断装置 |
| Product type | Medical device |
| Device class (Japan) | Class II |
| Approval, certification or notification number | 226AABZX00049000 |
| JMDN codes | 37642020 |
| Category code | A0900 |
| Marketing authorization holder | 製造販売／朝日レントゲン工業株式会社 |
| Package insert date | Aug 23, 2022 |
| 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: