Primary Device ID | 03700512916185 |
NIH Device Record Key | bf8bdf39-6c98-4cff-a10e-40402ac4b81b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MORPHEUS PUMP TUBE SET |
Version Model Number | ONG7435ST276 |
Catalog Number | 7435 |
Company DUNS | 401020409 |
Company Name | Promepla |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700512906186 [Primary] |
GS1 | 03700512916185 [Package] Contains: 03700512906186 Package: Box 1 [25 Units] In Commercial Distribution |
GS1 | 03700512926184 [Package] Contains: 03700512906186 Package: Box 2 [200 Units] In Commercial Distribution |
GBX | Catheter, Irrigation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-10 |
Device Publish Date | 2022-11-02 |