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DEUTSCH
ENGLISH
FRANÇAIS
ITALIANO
ESPAÑOL
NEDERLANDS
PORTUGUÊS
SVENSKA
DEUTSCH
ENGLISH
FRANÇAIS
ITALIANO
ESPAÑOL
NEDERLANDS
PORTUGUÊS
SVENSKA
© HAAG‑STREIT AG, 3098 Koeniz, Switzerland ‑ HS‑Doc. no. 1500.7220590‑04090 – 2021 – 08
10.1 Accessories / functionals parts / detachable parts /
consumables
Components
REF
Contrast enhancing filter (yellow) BP 900
1007839
Eyepiece 10x with reticule for estimating length and angle (BM900). To
be used in combination with 7220737
1400265
Eyepiece 12.5x for estimating length
1400302
Eyepiece 12.5x with crosshair reticule
3000470
Eyepiece 12.5x with dioptre adjustment
1400303
Eyepiece 12.5x with McIntyre comparison grid
1400304
Imaging module IM 600 BP
7220539
Breath shield (slit lamp BQ/BM/BP)
1007129
Protection shield large (for BP 900)
7221002
Short mirror
1001591
Fine brush for cleaning the optics
1001398
Diagnostic contact lenses
Please refer to the instructions for use 'Contact
lenses, Goldmann/Diagnostics/Laser'
Applanation Tonometer
Please refer to the instructions for use 'Applanation
tonometer AT 900 / AT 870' and 'Applanation
tonometer AT 900 D'
Headrest
Please refer to the instructions for use 'Headrest'
10.2 Legal regulations
• This device was developed and designed taking the EN 60601-1, EN ISO 10939
and EN ISO 15004-2 standards into account.
• The EN 60601-1 standard must be observed when using different medical and/
or non-medical electrical devices in combination.
• Compliance of the device with the Medical Device Regulation 2017/745 is
confirmed by the CE-designation.
• The device satisfies the electromagnetic compatibility requirements of EN
60601-1-2. The device has been designed to maintain the emissions of
electromagnetic interference at a level which does not exceed the statutory
guidelines and which does not affect other devices in its vicinity.
• The device also has the immunity stipulated by the standard.
• You can request a copy of the declaration of conformity for this device from
Haag-Streit at any time.
• Statutory accident regulations are to be observed.
10.3 Classification
Standard EN 60601-1
Protection class I
Operating mode
Continuous operation
CE Medical Device Regulation
2017/745
Class I
FDA
Class II
10.4 Disposal
Electrical and electronic devices must be disposed of separately from
household waste! This device was made available for sale after the
13th August 2005. For correct disposal, please contact your Haag-
Streit representative. This will guarantee that no hazardous
substances enter the environment and that valuable raw materials are
recycled.
10.5 Observed standards
EN 60601-1
EN 60601-1-2
EN ISO 10939
EN ISO 15004-2