Primary Device ID | 04038917411820 |
NIH Device Record Key | 4a129529-e2e1-4ff0-b81c-0ca5cea9b0fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biosphere® Screw Cap, blue |
Version Model Number | 65.716.221 |
Catalog Number | 65.716.221 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 50 |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04038917411813 [Primary] |
GS1 | 04038917411820 [Unit of Use] |
KDT | Container, Specimen Mailer And Storage, Sterile |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-04 |
Device Publish Date | 2025-07-25 |
04038917277730 | 65.716.201 |
04038917411820 | 65.716.221 |