Primary Device ID | 08718455508270 |
NIH Device Record Key | 1f173819-bbd8-4370-a902-ed3105ea2fe3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MED pro Medical B.V. |
Version Model Number | MD6/16 |
Company DUNS | 490059139 |
Company Name | MED pro Medical B.V. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Length | 9 Centimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08718455508270 [Primary] |
KOE | Dilator, Urethral |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-19 |
Device Publish Date | 2022-09-09 |