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date
08/05/2022
page 1 of 3
MODEL: GF1004M | DESCRIPTION: SPEAKER
FEATURES
• 102.4 mm
• square frame
• 6.0 W
•8Ω
• ferrite magnet
• PET cone
SPECIFICATIONS
parameter
conditions/description
min
impedance
at 0.6 kHz, 1.0 V
6.8
resonant frequency (Fo)
at 1.0 V
184
input power
frequency response
typ
max
units
6.0
10.0
W
8
9.2
Ω
230
276
Hz
Fo
sound pressure level
at 1.0 W, 50 cm, avg at 0.4, 0.5, 0.6, 0.8 kHz
buzz, rattle, etc.
must be normal at sine wave
dimensions
102.4 x 102.4 x 36.5
magnet
ferrite
cone material
PET
terminal
solder eyelets
91
93
14,000
Hz
95
dB
6.9
weight
210.0
operating temperature
-25
hand soldering
for maximum 5 seconds
RoHS
yes
V
mm
400
cuidevices.com
420
g
60
°C
440
°C
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CUI DEVICES | MODEL: GF1004M | DESCRIPTION: SPEAKER
date 08/05/2022 | page 2 of 3
MECHANICAL DRAWING
units: mm
tolerance: ±0.8 mm
93.50
55.00
36.50
22.50
0.80
3.50
5.2X7.5
(4 PLCS)
102.40
116.00
0.2
+
-
FREQUENCY RESPONSE CURVE
parameter
conditions/description
potentiometer range
50 dB
rectifier
RMS
lower limit frequency
20 Hz
wr. speed
100 mm/sec
zero level
60 dB
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CUI DEVICES | MODEL: GF1004M | DESCRIPTION: SPEAKER
date 08/05/2022 | page 3 of 3
REVISION HISTORY
rev.
description
date
1.0
initial release
09/20/2006
1.01
brand update
05/18/2020
logo, datasheet style update
08/05/2022
1.02
The revision history provided is for informational purposes only and is believed to be accurate.
CUI Devices offers a one (1) year limited warranty. Complete warranty information is listed on our website.
CUI Devices reserves the right to make changes to the product at any time without notice. Information provided by CUI Devices is believed to be accurate
and reliable. However, no responsibility is assumed by CUI Devices for its use, nor for any infringements of patents or other rights of third parties which may
result from its use.
CUI Devices products are not authorized or warranted for use as critical components in equipment that requires an extremely high level of reliability. A
critical component is any component of a life support device or system whose failure to perform can be reasonably expected to cause the failure of the life
support device or system, or to affect its safety or effectiveness.
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