Primary Device ID | 07613336155790 |
NIH Device Record Key | 6c6a64bd-5772-4ff5-84b1-e22d7a0d58ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AcfS L and D Equipment Installation Bundle |
Version Model Number | 07759274001 |
Catalog Number | 07759274001 |
Company DUNS | 117676383 |
Company Name | Roche Molecular Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613336155790 [Primary] |
JQW | STATION, PIPETTING AND DILUTING, FOR CLINICAL USE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-07 |
Device Publish Date | 2025-01-30 |
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