| Primary Device ID | 04823097717721 |
| NIH Device Record Key | 4ca5379b-71d2-43de-911f-d88d6ad2e67d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TM "Rehabilitimed" GL-1 XXXL Comfort |
| Version Model Number | GL-1 XXXL Comfort |
| Catalog Number | GL-1 XXXL Comfort |
| Company DUNS | 364875768 |
| Company Name | REABILITIMED TOV |
| 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 | 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 |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com | |
| Phone | 835 5030395 |
| Krut.Lora@gmail.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04823097717721 [Primary] |
| QSB | Orthosis, Truncal, Pregnancy |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-13 |
| Device Publish Date | 2025-05-05 |
| 04823097718933 | It is a beige bandage. It is made of elastic bandage fabric, reinforced with two stiffening ribs |
| 04823097717721 | It is a graphite color bandage. It is made of elastic bandage fabric, reinforced with two stiffe |