Primary Device ID | 10818614021215 |
NIH Device Record Key | 11e0584a-f134-4b84-9614-531be77da9b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tri-Gate Notched Disposable Cannula |
Version Model Number | 00-85700 |
Company DUNS | 117630237 |
Company Name | Maruho Medical, Inc. |
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 | true |
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 | 00818614021218 [Primary] |
GS1 | 10818614021215 [Package] Contains: 00818614021218 Package: Box [6 Units] In Commercial Distribution |
GEA | Cannula, Surgical, General & Plastic Surgery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-18 |
Device Publish Date | 2022-05-10 |
00818614021379 - Apollo | 2024-06-05 Medial Suture Anchor with Needles, PEEK |
10818614022595 - Disposable Punch, 6.5 mm | 2024-06-05 Disposable Punch, 6.5 mm Pouch |
00818614022635 - ABS Med Distraction Pin | 2023-09-06 ABS Med Distraction Pin , 12MM Pouch |
10818614022649 - ABS Med Distraction Pin | 2023-09-06 ABS Med Distraction Pin, 14MM Patient (Inner) |
10818614021406 - Distraction Screw | 2023-06-02 Distraction Screw, 12MM Patient (Inner) |
10818614021413 - Distraction Screw | 2023-06-02 Distraction Screw, 14MM Patient (Inner) |
10818614022601 - Distraction Pin, 12MM pouch | 2023-06-02 Sharp Distraction Pin, 12MM pouch |
10818614022618 - Distraction Pin, 14MM pouch | 2023-06-02 Sharp Distraction Pin, 14MM pouch |