This was resolved a couple of NEBS conferences ago. All the main RBOCs
were present and they agreed that a fuse was a special case. The fuse
is designed to open, therefore operation of the fuse is normal and allowed.
This may be a semantic strech, but that's where the current NEBS
Yes, NATA has informed us that the RTA list is being updated soon.
Curtis-Straus (USA) is also accredited to perform testing to AS/ACIF S043.
Jon Curtis
Kevin Richardson wrote:
Kristiaan,
Equipment which falls under TLN Category A50 is required to comply
with ACA TS001:1997 (Compliance
See laser notice 50 from the FDA.
http://www.fda.gov/cdrh/radhlth/laser.html
It's allowed, but you have to change the certification statement to
indicate that you are using the notice.
Jon Curtis
Curtis-Straus LLC
John Juhasz wrote:
I tried looking real hard for free downloadable ANSI
under the CDRH rules.
Jon Curtis
Curtis-Straus LLC
Davis, Mike wrote:
I agree with Doug and with John but, I have the same question. And I will
add, Doug is speaking of the FDA-CDRH requirement for the US. But, to
ascertain what the European mode is, this requires a single-fault condition
, you need to consider where the fiber goes as a break
might occur downstream and expose not only direct users of the equipment.
Jon Curtis
Curtis-Straus LLC
Doug Mckean wrote:
Do the acid test type question ...
During normal use, what are you exposing the end user to?
For instance
Go to
http://www.fda.gov/cdrh/radhlth/laser.html
and check out the reporting guides on product reports and annual reports.
Jon Curtis.
jsarell...@tuvam.com wrote:
Hello Group,
Does anyone know what is the procedure to follow for laser report
submittals to the CDRH?
this is not a medical
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