PMDA device listing
眼内プローブ
PMDA Medical device listing · 22200BZX00519000 · Class III
Key facts
| PMDA document key | 150176_22200BZX00519000_A_02 |
|---|---|
| Brand names | 眼内プローブ |
| General names (JMDN) | 眼科用レーザ光凝固装置滅菌済みプローブ |
| Product type | Medical device |
| Device class (Japan) | Class III |
| Approval, certification or notification number | 22200BZX00519000 |
| JMDN codes | 70640000 |
| Category code | A3100 |
| Marketing authorization holder | 製造販売／ディーマー・メディカル・ジャパン株式会社 |
| Package insert date | Dec 1, 2023 |
| PMDA product page | pmda.go.jp |
| Package insert on pmda.go.jp | pmda.go.jp |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- Listed Listed on the PMDA site
- Yes 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: