| Primary Device ID | 04946329385861 | 
| NIH Device Record Key | a1bbd433-4f84-473e-8341-11d0911e8ae2 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Narrow head section | 
| Version Model Number | 08-083-70 | 
| Catalog Number | 08-083-70 | 
| Company DUNS | 690677802 | 
| Company Name | MIZUHO CORPORATION | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| MRI Safety Status | Labeling does not contain MRI Safety Information | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | false | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | true | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | |
| Phone | 9999999999 | 
| regulatory@mizuho.co.jp | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Length | 254 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 04946329385861 [Primary] | 
| GDC | Table, Operating-Room, Electrical | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2025-09-15 | 
| Device Publish Date | 2025-09-05 | 
| 04946329219074 | Narrow Head Section (R2) | 
| 04946329219067 | Narrow Head Section (R1) | 
| 04946329385861 | 110 mm Pad for Narrow Head Section | 
| 04946329385854 | 70 mm Pad for Narrow Head Section | 
| 04946329385847 | Narrow Head Section |