Primary Device ID | 10816513022708 |
NIH Device Record Key | d944a06b-7b4d-45fe-897a-ee15a6ea9ce3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Set, I.V. Fluid Transfer |
Version Model Number | 17789HP3M-10PK |
Company DUNS | 079636164 |
Company Name | MPS 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816513022701 [Primary] |
GS1 | 10816513022708 [Package] Contains: 00816513022701 Package: BOX [10 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 | 2019-03-20 |
Device Publish Date | 2019-03-12 |
00816513022299 | SM-016 |
00816513022091 | MS550 |
00816513021704 | HR-012 |
00816513020271 | 3 PHARM-6 |
00816513020257 | 2 PHARM-6 |
00816513020240 | 19TPV |
00816513020196 | 19MMTP-B |
00816513020189 | 19MMTP |
00816513020172 | 19DTP-B |
00816513020080 | 17A-MTP |
00816513020066 | 17789HP3M |
00816513020059 | 17789HP |
00816513020042 | 17788HP3M |
00816513020035 | 17787HP3M |
00816513020028 | 1 PHARM-6FG |
00816513020011 | 1 PHARM-6 |
10816513023880 | KMI-LTP |
10816513024870 | 19DTP |
10816513025020 | NP-020 |
10816513025013 | NP-019 |
10816513025037 | NP-021 |
10816513024108 | HR-045 |
10816513023453 | NP-006 |
10816513023415 | NP-005 |
10816513022708 | 17789HP3M-10PK |
10816513025174 | MT-001 |
10816513023422 | BG-006-08 |