Primary Device ID | 15055140701173 |
NIH Device Record Key | 38f667ca-df7a-44c7-b374-cf61a78bac84 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Morpheus |
Version Model Number | 7435 |
Company DUNS | 228480810 |
Company Name | MEDIPLUS LTD |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +4401494551200 |
help@mediplus.co.uk |
Length | 3.4 Meter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05055140701176 [Primary] |
GS1 | 15055140701173 [Package] Contains: 05055140701176 Package: [25 Units] In Commercial Distribution |
FEN | DEVICE, CYSTOMETRIC, HYDRAULIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-16 |
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