Primary Device ID | 05407010126150 |
NIH Device Record Key | 05a18c85-6011-435a-ad8f-3eaa1ffdd5ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Polyethylene Glycol sup (4.4g container) |
Version Model Number | BESP1127J |
Catalog Number | BESP1127J |
Company DUNS | 370158847 |
Company Name | Lonza Verviers |
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 | false |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05407010126150 [Primary] |
JSK | Supplement, Culture Media |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-28 |
Device Publish Date | 2025-03-20 |
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05407010126150 - Polyethylene Glycol sup (4.4g container) | 2025-03-28 |
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