I cannot determine if the requirement for "identification" or "tracibility",
as per the context of the EMC and LV directives, pertains to use for a
recall, or just so the mfr is known.

Does anyone have the actual requirement, in either directive, for marking
with a batch or serial for the purpose of recall ?

This is what I have found for the LVD :

170. Section III
171. Information Requirements
172.
173. (a) Equipment shall be identified either by means of type, batch,
serial number or any other information allowing for the identification of
the product and for the traceability of the manufacturer. This shall be
marked legibly and indelibly on the equipment or, if this is not possible,
in the accompanying instructions for use. This identification shall be
amended accordingly if the equipment is altered in respect of the essential
health and safety requirements of this Directive.

> -----Original Message-----
> From: [email protected] [mailto:[email protected]]On Behalf Of John
> Woodgate
> Sent: Tuesday, February 06, 2007 7:23 AM
> To: [email protected]
> Subject: Re: DoCs After July
> But the product itself needs a serial or batch number, or
> perhaps a date
> code. This is a requirement of the LVD as well (in case a recall is
> necessary).

-

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