Primary Device ID | 04823097716953 |
NIH Device Record Key | a9e99a65-f566-4e53-ab97-ab7a719056a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TM "Rehabilitimed" L-4M-2 S Comfort |
Version Model Number | L-4M-2 S Comfort |
Catalog Number | L-4M-2 S 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 | 04823097716953 [Primary] |
MRI | Orthosis, Truncal/Orthosis, Limb |
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 |
04823097719626 | The beige orthopedic device for the lumbar spine, 24 cm high, is made of elastic bandage fabric |
04823097716953 | The graphite color orthopedic device for the lumbar spine, 24 cm high, is made of elastic bandag |