Primary Device ID | B54111267260 |
NIH Device Record Key | f5e8e57e-6b35-4dee-b570-ec2eb2c8c9dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QD Combo |
Version Model Number | QD Combo aluminum |
Catalog Number | 1126726 |
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 | B54111267260 [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 |
B54111267260 | QD Combination leg splints with aluminum ratchet, 1 QD-4 and 1 QD-3 splints |
B54111267160 | QD Combination leg traction splints with molded ratchet, 1 QD-4 and 1 QD-3 splints |