QD-4 Traction Splint 1126524

GUDID B54111265240

QD-4 Leg Traction Splint with aluminum ratchet, Adult/Pedi

FARETEC, INC.

First aid limb splint, non-mouldable, reusable
Primary Device IDB54111265240
NIH Device Record Key8c75b4d9-1f6a-41c6-9d94-174e071e23c0
Commercial Distribution StatusIn Commercial Distribution
Brand NameQD-4 Traction Splint
Version Model NumberAdult/Pedi, Aluminum
Catalog Number1126524
Company DUNS626802540
Company NameFARETEC, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com
Phone440-350-9510
Emailcolleen@faretec.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB54111265240 [Primary]

FDA Product Code

HSPSplint, Traction

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-08
Device Publish Date2020-08-31

On-Brand Devices [QD-4 Traction Splint]

B54111265240QD-4 Leg Traction Splint with aluminum ratchet, Adult/Pedi
B54111265140QD-4 Leg Traction Splint with molded ratchet, Adult/Pedi

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