| Primary Device ID | DHT15292 |
| NIH Device Record Key | c67188d0-f5d8-48ad-aba4-4fce7c5d5189 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aimsco |
| Version Model Number | 529 |
| Company DUNS | 008597056 |
| Company Name | DELTA HI TECH INC |
| Device Count | 10 |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | DHT15290 [Unit of Use] |
| HIBCC | DHT15291 [Primary] |
| HIBCC | DHT15292 [Package] Contains: DHT15291 Package: [10 Units] In Commercial Distribution |
| FMF | Syringe, Piston |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[DHT15292]
Ethylene Oxide
[DHT15292]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-01-06 |
| DHT17442 | 744 |
| DHT17422 | 742 |
| DHT17402 | 740 |
| DHT17222 | 722 |
| DHT16202 | 620 |
| DHT16182 | 618 |
| DHT15292 | 529 |
| DHT15282 | 528 |
| DHT15272 | 527 |
| DHT15262 | 526 |
| DHT15032 | 503 |
| DHT15022 | 502 |
| DHT16322 | 632 |
| DHT16312 | 631 |
| DHT16302 | 630 |
| DHT16222 | 622 |
| DHT16330 | Aimsco 32G 5/32 in Pen Needle |
| DHT16260 | Aimsco 29g 5/16" (8mm) Safety Pen Needle |
| DHT16250 | Aimsco 29g 3/16" (5mm) Safety Pen Needle |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AIMSCO 88815264 not registered Live/Pending |
Delta Hi-Tech, Inc. 2020-02-28 |