AccessGUDID - DEVICE: Cycle Tracking 4.0 (00194253312512)

GUDID

Device Identifier (DI) Information

Brand Name: Cycle Tracking 4.0
Version or Model: Feature Version 4.x
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: APPLE INC.

Primary DI Number: 00194253312512
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 060704780 *Terms of Use

Device Description: Cycle Tracking Watch App (Version 4.0)

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):	Yes
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?
64008	Menstrual cycle self-monitoring software	An interpretive software application intended to be used on a non-medical computerized device to allow a healthy woman to monitor the fertile and infertile phases of her menstrual cycle in the home, to assist her in achieving natural conception or prevent undesired pregnancy. It uses the symptothermal method which is based on data from self-observed signs such as waking temperature, the nature of cervical secretions, and cervix position/hardness.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LHD	Device, Fertility Diagnostic, Proceptive

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: 18c1f2d6-1274-4029-8e19-346fffc407cd
Public Version Date: November 11, 2024
Public Version Number: 1
DI Record Publish Date: November 01, 2024

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

[?]

No Customer Contact currently defined

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