Primary Device ID | B54111265240 |
NIH Device Record Key | 8c75b4d9-1f6a-41c6-9d94-174e071e23c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QD-4 Traction Splint |
Version Model Number | Adult/Pedi, Aluminum |
Catalog Number | 1126524 |
Company DUNS | 626802540 |
Company Name | FARETEC, INC. |
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 | 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 | false |
OTC Over-The-Counter | false |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com | |
Phone | 440-350-9510 |
colleen@faretec.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B54111265240 [Primary] |
HSP | Splint, Traction |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-08 |
Device Publish Date | 2020-08-31 |
B54111265240 | QD-4 Leg Traction Splint with aluminum ratchet, Adult/Pedi |
B54111265140 | QD-4 Leg Traction Splint with molded ratchet, Adult/Pedi |