Primary Device ID | DHT16250 |
NIH Device Record Key | b14154be-60df-413c-906f-e8b4e215e6d8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aimsco |
Version Model Number | 625 |
Company DUNS | 008597056 |
Company Name | DELTA HI TECH INC |
Device Count | 100 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | DHT16250 [Unit of Use] |
HIBCC | DHT16252 [Primary] |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-12 |
Device Publish Date | 2022-05-04 |
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 |