PRESTIGEPRO 6442

GUDID 10840490800059

Stretch Tourniquets, 1in x 18in, Blue, Single Use, Non-Sterile, Textured, 250 per bag

PRESTIGE AMERITECH, LTD.

Venous tourniquet, single-use
Primary Device ID10840490800059
NIH Device Record Keyfa553957-b2cd-436f-bec2-a8a9f96d3d55
Commercial Distribution StatusIn Commercial Distribution
Brand NamePRESTIGEPRO
Version Model Number6442
Catalog Number6442
Company DUNS199692794
Company NamePRESTIGE AMERITECH, LTD.
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 Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, avoid direct sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100840490800052 [Primary]
GS110840490800059 [Package]
Contains: 00840490800052
Package: case [4 Units]
In Commercial Distribution

FDA Product Code

GAXTourniquet, Nonpneumatic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-14
Device Publish Date2025-04-04

On-Brand Devices [PRESTIGEPRO]

10840490800066Stretch Tourniquets, 1in x 18in, Orange, Single Use, Non-Sterile, Textured, 250 per bag
10840490800059Stretch Tourniquets, 1in x 18in, Blue, Single Use, Non-Sterile, Textured, 250 per bag
00840490800045Stretch Tourniquets, 1in x 18in, Blue, Single Use, Non-Sterile, Textured, Perforated Roll, 25 pe
10840490800035Stretch Tourniquets, 1in x 18in, Blue, Single Use, Non-Sterile, Rolled and Banded, 100 per bag
10840490800028Stretch Tourniquets, 1in x 18in, Orange, Single Use, Non-Sterile, Textured, 250 per box
10840490800011Stretch Tourniquets, 1in x 18in, Blue, Single Use, Non-Sterile, Textured, 250 per box
00840490800007Stretch Tourniquets, 1in x 18in, Blue, Single Use, Non-Sterile, Textured, 25 per roll

Trademark Results [PRESTIGEPRO]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PRESTIGEPRO
PRESTIGEPRO
98824447 not registered Live/Pending
Prestige Ameritech Ltd.
2024-10-28
PRESTIGEPRO
PRESTIGEPRO
87881078 not registered Dead/Abandoned
Prestige Employee Administrators, Inc.
2018-04-17

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.