Primary Device ID | 10810080610412 |
NIH Device Record Key | b7ce88da-48d1-4afe-b880-acc684fffe8b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXTENSION SET |
Version Model Number | EI-060-02 |
Company DUNS | 117970217 |
Company Name | MPS Pharma & Medical, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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 | 00810080610415 [Primary] |
GS1 | 10810080610412 [Package] Contains: 00810080610415 Package: Case [50 Units] In Commercial Distribution |
LHI | Set, I.V. Fluid Transfer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-01 |
Device Publish Date | 2022-08-24 |
10810080611662 | EA-060-01 |
10810080610412 | EI-060-02 |
10810080610405 | EG-060-01 |
10810080610399 | EG-014-01 |
10810080610382 | ED-030-01 |
10810080610375 | EC-072-01 |
10810080610368 | EC-060-01 |
10810080610351 | EB-096-01 |
10810080610344 | EB-072-03 |
10810080610337 | EB-072-02 |
10810080610313 | EB-060-03 |
10810080610306 | EB-060-02 |
10810080610290 | EB-060-01 |
10810080610276 | EB-038-11 |
10810080610252 | EB-030-13 |
10810080610245 | EB-030-02 |
10810080610238 | EB-012-01 |
10810080610221 | DB-006-05 |