Primary Device ID | 20896128002033 |
NIH Device Record Key | 3b0d13c3-c5c9-41ad-9b20-e9e23557e14b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FMS2000 ACCESSORY |
Version Model Number | 903-00013 |
Company DUNS | 078330362 |
Company Name | BELMONT INSTRUMENT CORPORATION |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20896128002033 [Primary] |
FRN | Pump, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
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