Primary Device ID | 05708590389875 |
NIH Device Record Key | fde5930c-5501-4877-88ab-7c229426f242 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MCT 5 |
Version Model Number | R95027 |
Catalog Number | R9502719000 |
Company DUNS | 305656662 |
Company Name | Pressalit A/S |
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 | true |
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 | 05708590389875 [Primary] |
INW | Table, Mechanical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-13 |
Device Publish Date | 2024-11-05 |
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