| Primary Device ID | 00841912102501 |
| NIH Device Record Key | e3f99e79-f3f0-463f-9832-1d73aa3ff90b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reusable Stainless Steel Endocavity Needle Guide |
| Version Model Number | 6131 |
| 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 | 00841912102501 [Direct Marking] |
| GS1 | 10841912102508 [Primary] |
| ITX | Transducer, Ultrasonic, Diagnostic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00841912102501]
Moist Heat or Steam Sterilization
[00841912102501]
Moist Heat or Steam Sterilization
[00841912102501]
Moist Heat or Steam Sterilization
[00841912102501]
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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