Aveta Waste Bag 205-2000

GUDID 00850006759378

Aveta Waste Bag (with cap), for use with Aveta System

MEDITRINA, INC.

Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile Surgical tissue/fluid collection bag, non-sterile
Primary Device ID00850006759378
NIH Device Record Keyf63d0c4a-4024-403b-aeb3-0f7f0cbced35
Commercial Distribution StatusIn Commercial Distribution
Brand NameAveta Waste Bag
Version Model Number205-2000
Catalog Number205-2000
Company DUNS080570262
Company NameMEDITRINA, 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100850006759361 [Primary]
GS100850006759378 [Package]
Contains: 00850006759361
Package: shelf carton [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HIHHysteroscope (And Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-01
Device Publish Date2021-01-22

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