Latch 20IL340310
GUDID 00841439102046
for use with Philips GEMINI system
MEDTEC, INC.
Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system Indexed-immobilization patient positioning system| Primary Device ID | 00841439102046 |
| NIH Device Record Key | 868e8200-bce7-4fbd-af68-a55fc16e6a14 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Latch |
| Version Model Number | 20IL340310 |
| Catalog Number | 20IL340310 |
| Company DUNS | 103977526 |
| Company Name | MEDTEC, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
| Width | 20 Centimeter |
| Length | 25 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841439102046 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K973842
FDA Product Code
| IXQ | Table, radiographic, stationary top |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-03-19 |
| Device Publish Date | 2017-08-02 |
On-Brand Devices [Latch]
| 00841439102046 | for use with Philips GEMINI system |
| 00841439100417 | Latch |
Trademark Results [Latch]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LATCH 97718370 not registered Live/Pending |
WRx Nutrition, LLC 2022-12-15 |
 LATCH 97225082 not registered Live/Pending |
Jung, Min-Kyu 2022-01-18 |
 LATCH 90715486 not registered Live/Pending |
Katherine Ramos 2021-05-17 |
 LATCH 88333287 not registered Live/Pending |
Latchable, Inc. 2019-03-10 |
 LATCH 88333285 not registered Live/Pending |
Latchable, Inc. 2019-03-10 |
 LATCH 86975928 4729308 Live/Registered |
Munchkin, Inc. 2013-10-22 |
 LATCH 86871386 5026399 Live/Registered |
Oakley, Inc. 2016-01-11 |
 LATCH 86837452 4961853 Live/Registered |
Latchable, Inc. 2015-12-02 |
 LATCH 86502812 4928776 Live/Registered |
Munchkin, Inc. 2015-01-14 |
 LATCH 86502492 4794850 Live/Registered |
Munchkin, Inc. 2015-01-13 |
 LATCH 86097968 not registered Dead/Abandoned |
Munchkin, Inc. 2013-10-22 |
 LATCH 85912775 4539967 Live/Registered |
Munchkin, Inc. 2013-04-23 |
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