As part of listing your products on the Baby Bunting Marketplace, we will request test reports conforming with the safety and compliance standards set by regulatory bodies in Australia.
Furthermore, any claims, such as greenwashing claims, about a product must be supported by a report or claim substantiation certificate from the manufacturer or supplier (wherever applicable), and you may refer to our Marketplace Advertising Guidelines for more information.
Baby Bunting will conduct regular audits and may request additional information to verify the safety and compliance of your products. If this information is not provided within a given timeline, Baby Bunting has the authority to remove your products from our website under clause 4.5 of the Marketplace participation agreement.
Test Report and Compliance Document Criteria:
- Please note that the compliance and safety standard test reports submitted should not be more than three years old.
- The reports need to be in AU format/standards or in a format that suffices AU standards.
ELECTRIC/WEARABLE BREAST PUMP
Mandatory Requirements
- The product should be registered in TGA (Therapeutic Goods of Administration). Provide the ARTG number. (if the product is a medical device)
- Submit a test report showing compliance with the following standards:
- EN 55014-1:2021 - Electromagnetic compatibility
- EN 55014-2: 2021 - Electromagnetic compatibility
- BS EN IEC 61000-3-3:2013 - EMC
- EN 60335-1 - Household and similar electrical appliances - Safety - Part 1: General
- requirement
- ETSI EN 300 328 V2.2.2 - Wideband transmission systems
- BPA testing on parts that come in contact with food items
MANUAL BREAST PUMP
Mandatory Requirement
- The product should be registered in TGA (Therapeutic Goods of Administration). Provide the ARTG number. (if the product is a medical device)
BREAST PUMP ACCESSORIES
e.g. Inserts, Breast shields, connector, collection cup
- The product should be registered in TGA (Therapeutic Goods of Administration). Provide the ARTG number. (if the breastpump is a medical device)
COLD and HOT GEL PACK
Mandatory Requirement
- The product should be registered in TGA (Therapeutic Goods of Administration). Provide the ARTG number.
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