AccessGUDID - DEVICE: Avalon Fetal Monitor FM30 (00884838000414)

GUDID

Device Identifier (DI) Information

Brand Name: Avalon Fetal Monitor FM30
Version or Model: Avalon FM30 Fetal Monitor
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 862199
Company Name: Philips Medizin Systeme Böblingen GmbH

Primary DI Number: 00884838000414
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 314101143 *Terms of Use

Device Description: Avalon FM30 Fetal Monitor for all external and internal Fetal Monitoring Applications including: 1US Transducer and 1 Toco Transducer, MECG Adapter Cable and DECG Reusable Legplate Adapter Cable and the capability of measuring DECG, MECG and IUP

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
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):	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?
37796	Foetal/maternal prenatal monitor	An electrically-powered device designed for continuous monitoring of foetal heart activity and maternal uterine contractions during the prenatal (commonly perinatal) period; it may monitor additional maternal parameters [e.g., electrocardiogram (ECG), noninvasive blood pressure (NIBP), pulse oximetry (SpO2)]. Also known as a cardiotocograph, uterine contractions are acquired using a tocodynamometer (pressure transducer) strapped onto the mother's abdomen, while foetal heart rate is typically measured with a dedicated ultrasound transducer. The results may be displayed via print-out or electronically; telemetry features may also be included.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HGM	SYSTEM, MONITORING, PERINATAL

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: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between -20 and 60 Degrees Celsius
Storage Environment Temperature: between -4 and 140 Degrees Fahrenheit
Storage Environment Atmospheric Pressure: between 57 and 106 KiloPascal
Storage Environment Humidity: between 15 and 90 Percent (%) Relative Humidity

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: c8c0bf3c-e7bd-4fd6-a3aa-cd353fa08eb8
Public Version Date: May 05, 2023
Public Version Number: 8
DI Record Publish Date: October 03, 2016