TRA MEDICAL AND DENTAL SUPPLY

GUDID 20809160106508

MEDICAL ACTION INDUSTRIES INC.

Suture removal kit
Primary Device ID20809160106508
NIH Device Record Key7b655d01-0a5e-4c4b-9ac0-61fd9bf328aa
Commercial Distribution Discontinuation2019-09-30
Commercial Distribution StatusNot in Commercial Distribution
Brand NameTRA MEDICAL AND DENTAL SUPPLY
Version Model Number70226
Company DUNS092364462
Company NameMEDICAL ACTION INDUSTRIES INC.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0

Device Identifiers

Device Issuing AgencyDevice ID
GS110809160106501 [Primary]
GS120809160106508 [Package]
Contains: 10809160106501
Package: [50 Units]
Discontinued: 2019-09-30
Not in Commercial Distribution

FDA Product Code

MCZSuture removal kit

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-01
Device Publish Date2016-09-22

Devices Manufactured by MEDICAL ACTION INDUSTRIES INC.

20809160423896 - Medical Action Industries2024-04-25
20809160423902 - Medical Action Industries2024-04-25
20809160423919 - Medical Action Industries2024-04-25
20809160423926 - Medical Action Industries2024-04-25
20809160423933 - Medical Action Industries2024-04-25
20809160423780 - Medical Action Industries2024-04-24
20809160423803 - Medical Action Industries2024-04-24
20809160423605 - Medical Action Industries2024-04-23

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