AccessGUDID - DEVICE: Monoject (10884527002993)

GUDID

Device Identifier (DI) Information

Brand Name: Monoject
Version or Model: 8881310240
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 8881310240
Company Name: Cardinal Health, Inc.

Primary DI Number: 10884527002993
Issuing Agency: GS1
Commercial Distribution End Date: June 30, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 080935429 *Terms of Use

Device Description: Blood Collection Tube,Glycerine Coated Lavender Stopper, EDTA (NA2) 4.5 mg, 3 mL Draw

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
37563	Non-evacuated blood collection tube IVD, no additive	A non-evacuated glass or plastic tube, sealed with a stopper, containing no additive and intended to be used for the collection, and preservation and/or transport, of blood for analysis and/or other investigation. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GIM	Tubes, vacuum sample, with anticoagulant

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Keep dry; Fragile;AVOID DIRECT SUNLIGHT

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 10.25 Millimeter
Total Volume: 3 Milliliter
Length: 64 Millimeter

Device Record Status

Public Device Record Key: 87727e28-f2a6-4df2-8072-0b3de471e2dc
Public Version Date: June 30, 2023
Public Version Number: 9
DI Record Publish Date: October 13, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
20884527002990	100	10884527002993	2023-06-30	Not in Commercial Distribution	PACK_OR_INNER_PACK
30884527002997	1000	10884527002993	2023-06-30	Not in Commercial Distribution	CASE