Primary Device ID | 04946329402537 |
NIH Device Record Key | 73fe29a7-a81d-4885-8ade-1c6446eda8e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spatula |
Version Model Number | 07-959-21 |
Catalog Number | 07-959-21 |
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 |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04946329402537 [Primary] |
HAO | Instrument, Surgical, Non-Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
[04946329402537]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-30 |
Device Publish Date | 2023-05-22 |
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 |