Primary Device ID | 00840117310223 |
NIH Device Record Key | ce07d189-9d3a-4076-87ad-818bd39c54c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pulse Oximeter |
Version Model Number | 36402 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
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 | 00840117310223 [Primary] |
GS1 | 00840117310230 [Package] Package: Master Case [10 Units] In Commercial Distribution |
GS1 | 00840117336230 [Package] Contains: 00840117310230 Package: Shipper [1 Units] In Commercial Distribution |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-12-30 |
Device Publish Date | 2021-12-22 |
00616784709031 | 7090 |
00616784708935 | 7089 |
00616784708836 | 7088 |
00840117310223 | Pulse Oximeter, Pediatric |
00840117310162 | Pulse Oximeter |