ANA 70 Duett 400

GUDID 00853383006608

Wykle Research, Inc

Dental amalgam
Primary Device ID00853383006608
NIH Device Record Keyb5e3a308-8b30-4211-ae82-ab204719f49d
Commercial Distribution StatusIn Commercial Distribution
Brand NameANA 70 Duett 400
Version Model Number1116000
Company DUNS614557155
Company NameWykle Research, Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Operating and Storage Conditions

Handling Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100853383006608 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EJJAlloy, Amalgam

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-04-13

Devices Manufactured by Wykle Research, Inc

00853383006011 - Original D Capsules 1 Spill Fast Set 50 count2018-07-12
00853383006158 - Original D Tablets Fast Set 10 oz2018-07-12
00853383006202 - Original D Capsules 2 Spill Fast Set 100 count2018-07-12
00853383006035 - Wykalloy Capsules 1 Spill 50 count2018-07-06
00853383006042 - Wykalloy Capsules 2 Spill 50 count2018-07-06
00853383006059 - Wykalloy Capsules 3 Spill 50 count2018-07-06
00853383006066 - Wykalloy Capsules 1 Spill 500 count2018-07-06
00853383006073 - Wykalloy Capsules 2 Spill 500 count2018-07-06

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