AccessGUDID - DEVICE: Diamedix (00817273020280)

GUDID

Device Identifier (DI) Information

Brand Name: Diamedix
Version or Model: 720-480
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: DIAMEDIX CORPORATION

Primary DI Number: 00817273020280
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 151765328 *Terms of Use

Device Description: "720-480 anti-Cardiolipin Screen"

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:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	Yes
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?
52697	Anti-E [RH0003] antibody screen IVD, control	A material containing antibodies to E red blood cell antigens [RH0003] from the Rhesus system intended to be used in immunohaematological testing of a clinical specimen to verify the performance of an antibody screening assay that is used for detecting red cell alloantibodies.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JZO	System, Test, Thyroid Autoantibody

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K983553	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: eb11f4cc-0925-4eb1-ba4c-2770b12b7cc5
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: September 20, 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
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 305-324-2300
Email: customersupport@erbadiagnostics.com

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