Primary Device ID | 00857252004016 |
NIH Device Record Key | e8b4eda1-fc5a-466e-ad88-8063cf0ffa03 |
Commercial Distribution Discontinuation | 2020-01-24 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Accordion Stone Control Device; Accordion Stone Management Device |
Version Model Number | PA1305-01-10 |
Company DUNS | 101084796 |
Company Name | T H S INTERNATIONAL, 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857252004016 [Primary] |
FFL | Dislodger, Stone, Basket, Ureteral, Metal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-01-27 |
Device Publish Date | 2016-06-06 |
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