Primary Device ID | 20809160106508 |
NIH Device Record Key | 7b655d01-0a5e-4c4b-9ac0-61fd9bf328aa |
Commercial Distribution Discontinuation | 2019-09-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | TRA MEDICAL AND DENTAL SUPPLY |
Version Model Number | 70226 |
Company DUNS | 092364462 |
Company Name | MEDICAL ACTION INDUSTRIES INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | true |
Special Storage Condition, Specify | Between 0 and 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10809160106501 [Primary] |
GS1 | 20809160106508 [Package] Contains: 10809160106501 Package: [50 Units] Discontinued: 2019-09-30 Not in Commercial Distribution |
MCZ | Suture removal kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-01 |
Device Publish Date | 2016-09-22 |
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