Primary Device ID | 00841912102600 |
NIH Device Record Key | b7595fb5-228b-4893-b2e7-a198eb5f2f87 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reusable (Short Style) Stainless Steel Endocavity Needle Guide |
Version Model Number | 6390 |
Company DUNS | 965417181 |
Company Name | PROTEK MEDICAL PRODUCTS, 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 | false |
Lot Batch | true |
Serial Number | false |
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 | 00841912102600 [Direct Marking] |
GS1 | 10841912102607 [Primary] |
ITX | Transducer, Ultrasonic, Diagnostic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841912102600]
Moist Heat or Steam Sterilization
[00841912102600]
Moist Heat or Steam Sterilization
[00841912102600]
Moist Heat or Steam Sterilization
[00841912102600]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2016-09-16 |
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