Primary Device ID | 03700512977902 |
NIH Device Record Key | c588a574-9a35-4ceb-be32-3880ce5c0116 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Filter Basket |
Version Model Number | ROKT1800ST245 |
Catalog Number | FILT1800 |
Company DUNS | 401020409 |
Company Name | Promepla |
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 | 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 | 03700512967903 [Primary] |
GS1 | 03700512977902 [Package] Contains: 03700512967903 Package: Box 1 [1 Units] In Commercial Distribution |
GS1 | 03700512987901 [Package] Package: Box 2 [4 Units] In Commercial Distribution |
FFL | Dislodger, Stone, Basket, Ureteral, Metal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-04 |
Device Publish Date | 2021-02-24 |