4095000

GUDID 20884521162010

Ezee Nest Smpl Cup Roche

Cardinal Health, Inc.

Medicine cup, single-use

Primary Device ID	20884521162010
NIH Device Record Key	e1dc8240-a5b2-4204-aa51-7dd7a2e05d72
Commercial Distribution Discontinuation	2025-12-31
Commercial Distribution Status	In Commercial Distribution
Version Model Number	4095000
Catalog Number	4095000
Company DUNS	080935429
Company Name	Cardinal Health, Inc.
Device Count	1000
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Device Dimensions

Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter
Length	16 Millimeter

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521162013 [Primary]
GS1	20884521162010 [Package] Contains: 10884521162013 Package: CASE [5000 Units] Discontinued: 2025-12-31 In Commercial Distribution
GS1	30884521162017 [Unit of Use]

FDA Product Code

KYW	CONTAINER, LIQUID MEDICATION, GRADUATED

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2024-11-07
Device Publish Date	2018-06-27

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