35
Labelling and Symbols
This product is a certified Class IIa medical device and complies with the requirements of Directive
93/42/EEC, amended by 2007/47/EEC.
In accordance with IEC 60529 the International Protection rating is IP22 which relates to the degree of
waterproofing this product complies with.
This symbol is required by European directive 2002/96/EEC on waste electrical and electronic
equipment (WEEE). At the end of its useful life this device must not be disposed of as normal domestic
waste. Instead it must be delivered to a WEEE authorised collection centre. Due to the construction
materials used for the device, disposal as normal waste could cause harm to the environment and/or
health.
LOT
Indicates the lot number for this product 1712
-
02
-
00600.
This product is manufactured by Shenzhen Jumper Medical Equipment Co., Ltd, Building D, No 71,
Xintian Road, Fuyong Street, Baoan, Shenzhen, Guangdong Province, 518102, China .
SN
Device serial number.
Model
Digital Pulse Oximeter Monitor JPD
-
500F.
2 x AAA Alkaline Batteries.
Read instructions before use.
Date of Manufacture 2017
-
10.
Battery
FCC ID
Indicates the lot number for this product 2ADYL
-
JPD500F.
EC REP
European Representative: Wellkang Ltd, Suite B, 29 Harley Street, London, W1G 9QR, UK.
IP22
In accordance with IEC 60601
-
1 the product and its applied parts are type BF and thus protected
against the risks of electrical leakage.
