| Primary Device ID | 04946329389838 |
| NIH Device Record Key | 82beb2fe-c9c8-4d55-9cbe-2a4dcab8a064 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Spatula |
| Version Model Number | 07-959-01 |
| Catalog Number | 07-959-01 |
| 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 | false |
| 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 | |
| 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 | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Length | 200 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04946329389838 [Primary] |
| HAO | Instrument, Surgical, Non-Powered |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
[04946329389838]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-03-28 |
| Device Publish Date | 2023-03-20 |
| 04946329389852 | Spatula 2 mm Stainless |
| 04946329389845 | Spatula 4 mm Stainless |
| 04946329389838 | Spatula 6 mm Stainless |
| 04946329402605 | Spatula 140 mm x 20 mm, Stainless |
| 04946329402599 | Spatula 140 mm x 15 mm, Stainless |
| 04946329402582 | Spatula 140 mm x 10 mm, Stainless |
| 04946329402575 | Spatula 210 mm x 30 mm, Stainless |
| 04946329402568 | Spatula 210 mm x 20 mm, Stainless |
| 04946329402551 | Spatula 210 mm x 15 mm, Stainless |
| 04946329402544 | Spatula 210 mm x 10 mm, Stainless |
| 04946329402537 | Spatula 210 mm x 5 mm, Stainless |