Hummi Micro-Draw ABG-HM-1
GUDID 20817522013302
hummi micro draw
KENTEC MEDICAL, INC.
Arterial blood sampling kit| Primary Device ID | 20817522013302 |
| NIH Device Record Key | e31b36f9-47c6-444c-9921-fdf021867e2e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hummi Micro-Draw |
| Version Model Number | ABG-HM-1 |
| Catalog Number | ABG-HM-1 |
| Company DUNS | 066175613 |
| Company Name | KENTEC 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com | |
| Phone | 949-863-0810 |
| kjrooks@kentecmedical.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10817522013305 [Primary] |
| GS1 | 20817522013302 [Package] Contains: 10817522013305 Package: box [50 Units] In Commercial Distribution |
FDA Product Code
| KST | System, Blood Collection, Vacuum-Assisted, Manual |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-11 |
| Device Publish Date | 2021-06-03 |
Devices Manufactured by KENTEC MEDICAL, INC.
| 20817522013371 - Swabeze | 2024-07-08 foam swab |
| 20817522013357 - Swabeze | 2024-07-05 foam swab |
| 20817522013364 - Swabeze | 2024-07-05 foam swab |
| 20817522013388 - Swabeze | 2024-07-05 foam swab |
| 20817522013340 - Swabeze | 2024-06-28 low absorption foam swab |
| 20817522010356 - Ameritus | 2024-06-06 large size ecg electrode |
| 20817522010363 - Ameritus | 2024-06-06 small size ecg electrode |
| 20817522013333 - Kentec electrode | 2024-05-03 5-lead electrode |
Trademark Results [Hummi Micro-Draw]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HUMMI MICRO-DRAW 97516557 not registered Live/Pending |
Kentec Medical, Inc. 2022-07-22 |
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