HipFix® Thermoplastic MTHFX1822

GUDID 00841439104293

45.7 x 55.9cm standard perforated thermoplastic (3.2mm)

MEDTEC, INC.

Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material Patient positioning thermoplastic mould material
Primary Device ID00841439104293
NIH Device Record Keybc74f462-20f5-4c9a-9d02-179e0932ab12
Commercial Distribution StatusIn Commercial Distribution
Brand NameHipFix® Thermoplastic
Version Model NumberMTHFX1822
Catalog NumberMTHFX1822
Company DUNS103977526
Company NameMEDTEC, INC.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com
Phone+1(712)737-8688
Emailradiotherapy.complaints@civcort.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Storage Environment TemperatureBetween 0 and 100 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS100841439104293 [Package]
Contains: 10841439104290
Package: [5 Units]
In Commercial Distribution
GS110841439104290 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, linear, medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2020-04-01
Device Publish Date2017-09-25

On-Brand Devices [HipFix® Thermoplastic]

0084143910704145.7 x 55.9cm IMRT thermoplastic (3.2mm)
0084143910703445.7 x 55.9cm standard perforated thermoplastic (3.2mm)
0084143910702745.7 x 55.9cm solid thermoplastic (3.2mm)
0084143910432345.7 x 55.9cm solid thermoplastic (3.2mm)
0084143910431645.7 x 55.9cm solid thermoplastic (2.4mm)
0084143910430945.7 x 55.9cm standard perforated thermoplastic (2.4mm)
0084143910429345.7 x 55.9cm standard perforated thermoplastic (3.2mm)
0084143910428645.7 x 55.9cm IMRT thermoplastic (2.4mm)
0084143910427945.7 x 55.9cm IMRT thermoplastic (3.2mm)

Trademark Results [HipFix]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HIPFIX
HIPFIX
74661998 1961969 Live/Registered
MEDTEC, INC.
1995-04-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.