Primary Device ID | 05032384083237 |
NIH Device Record Key | 141ab731-13b4-4aea-a094-648b066fcd71 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OXACILLIN RES. SCREENING AGAR BASE |
Version Model Number | CM1008B |
Company DUNS | 365355452 |
Company Name | OXOID LIMITED |
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 | 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 | 05032384083237 [Primary] |
JSI | Culture Media, Selective And Differential |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-06 |
Device Publish Date | 2024-10-29 |
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05032384083237 - OXACILLIN RES. SCREENING AGAR BASE | 2024-11-06 |
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05032384002092 - Desoxycholate Citrate Agar (Hynes) | 2024-08-21 |