Primary Device ID | 04823097719831 |
NIH Device Record Key | f6974d04-443c-4044-820c-a5ec3d11d85f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TM "Rehabilitimed" GR-3P XXL Comfort |
Version Model Number | GR-3P XXL Comfort |
Catalog Number | GR-3P XXL 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 Issuing Agency | Device ID |
---|---|
GS1 | 04823097719831 [Primary] |
IPW | Orthosis, Sacroiliac, Soft |
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 |
04823097719831 | It is an inguinal hernia bandage, with a front fastener, beige in color. It is made of elastic f |
04823097717769 | It is an inguinal hernia bandage, with a front fastener, graphite color. It is made of elastic f |