Primary Device ID | 04038917361637 |
NIH Device Record Key | 0f39bc78-2374-4fd9-be0e-00caa938b7d8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multisealer MS 500M |
Version Model Number | 87.7708.850 |
Catalog Number | 87.7708.850 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 1 |
DM Exempt | true |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com | |
Phone | +1(800)257-5101 |
customerservice.us@sarstedt.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04038917361637 [Primary] |
KSD | Device, heat-sealing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-08 |
Device Publish Date | 2022-11-30 |
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04038917994590 - SC MTube 0,5 ml | 2024-12-06 |
04038917203050 - Srew cap Tobe 10 ml with Stabilur tablet | 2024-11-26 |
04038917992428 - 8,5 ml Urine Monovette | 2024-11-04 |