Primary Device ID | 04946329376302 |
NIH Device Record Key | 3ed5df32-2854-48fc-b3e1-1afbe9c5f5be |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sugita Titanium Clip II Metal Half Case |
Version Model Number | 17-010-26 |
Catalog Number | 17-010-26 |
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 | |
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 | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Length | 264 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04946329376302 [Primary] |
HBR | Rack, Clip |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
[04946329376302]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-11 |
Device Publish Date | 2022-02-03 |
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