AccessGUDID - DEVICE: Home Page (00858637005253)

GUDID

Device Identifier (DI) Information

Brand Name: Home Page
Version or Model: 2.0
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: EXACT SCIENCES CORPORATION

Primary DI Number: 00858637005253
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 150908853 *Terms of Use

Device Description: No description.

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):	No
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?
58047	Laboratory instrument application software IVD	An individual software program or group of programs, routines or algorithms that add specific data communication, display, processing and/or system integration capabilities to one or more pre-analytical laboratory processing functions (eg. robotic specimen transfer, aliquoting, pipetting, serial dilutions, reagent dispensing, etc) and assay processing functions (microplate washing, incubation control, plate agitation etc) using a series of programmable sequences and data communication facilities to achieve semi-automated throughput. The program applications are restricted to instrument operations and do not generally include data reduction, result interpretation or reporting facilities.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
PHP	System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
P130017	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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 51717a1e-4954-4e6b-885d-4ec39f55d57f
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: August 21, 2015

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: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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