BASIC
GUDID B845NGDM10433
Intco Medical Industries, Inc.
Nitrile examination/treatment glove, non-powdered, non-antimicrobial| Primary Device ID | B845NGDM10433 |
| NIH Device Record Key | 3eea535e-c45b-4741-b4aa-ebf8c3a617cc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BASIC |
| Version Model Number | NGDM1043 |
| Company DUNS | 080162537 |
| Company Name | Intco Medical Industries, 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 | true |
| 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 |
Customer Support Contacts
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com | |
| Phone | +862134978818 |
| maxli@intco.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B845NGDM1043 [Unit of Use] |
| HIBCC | B845NGDM10431 [Primary] |
| HIBCC | B845NGDM10433 [Package] Contains: B845NGDM10431 Package: [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K123869
FDA Product Code
| LZA | Polymer Patient Examination Glove |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-14 |
| Device Publish Date | 2024-02-06 |
On-Brand Devices [BASIC]
Trademark Results [BASIC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BASIC 98829463 not registered Live/Pending |
CAUTIVA ENTERPRISE LLC 2024-10-30 |
 BASIC 98703849 not registered Live/Pending |
Supmedic 2024-08-17 |
 BASIC 98703842 not registered Live/Pending |
Supmedic 2024-08-17 |
 BASIC 98649322 not registered Live/Pending |
Basic Medical Technology Inc. 2024-07-15 |
 BASIC 98423423 not registered Live/Pending |
Makita Corporation 2024-02-27 |
 BASIC 98374359 not registered Live/Pending |
Supmedics Inc. 2024-01-24 |
 BASIC 98140760 not registered Live/Pending |
Unsifted, Inc. 2023-08-18 |
 BASIC 98107666 not registered Live/Pending |
Supmedics Inc. 2023-07-28 |
 BASIC 97935514 not registered Live/Pending |
Ehaoyao International Trading Hong KongCompany Limited 2023-05-14 |
 BASIC 97624009 not registered Live/Pending |
Supmedics Inc. 2022-10-07 |
 BASIC 97422680 not registered Live/Pending |
Basic Lifestyle LLC 2022-05-21 |
 BASIC 90792769 not registered Live/Pending |
TARA BRANDS, LLC 2021-06-24 |
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