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Idiomas disponibles
9681 Clipper Specifications
Motor voltage:
Current without load:
Current with full load:
RPM:
Power adapters/charge circuits:
Charging time:
Battery operating time:
Battery:
Clipper weight (with blade):
Clipper dimensions (with blade):
THE DEVICE HAS BEEN TESTED IN ACCORDANCE WITH IEC 60601‑1 EDITION
3.1 (MEDICAL – GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL
PERFORMANCE) AND IEC‑60601‑1‑2 EDITIONS 3 AND 4 (COLLATERAL
STANDARD‑ELECTROMAGNETIC DISTURBANCES)
This device complies with the requirements of European Medical Device Directive 93/42/EEC.
ELECTROMAGNETIC ENVIRONMENT GUIDANCE
ELECTROMAGNETIC EMISSION
The 3M™ Surgical Clipper Professional, 9681 is intended for use in the electromagnetic
environment specified below. The customer or user of the 3M™ Surgical Clipper Professional,
9681 should ensure that it is used in such an environment.
Emissions Test
RF Emissions
CISPR 11
RF Emissions
CISPR 11
Harmonics
IEC 61000‑3‑2
Flicker
IEC 61000‑3‑3
3.6 volt DC
1.0 amps max.
1.3 amps max.
5500‑6500
All power adapters/charge circuits are 100‑240 VAC, 50‑60Hz
4 hours initial, 4 hours thereafter
~120 minutes
Lithium‑Ion (Li‑ion)
180 grams (6.7 oz)
15.5 cm (6.1 in.) length
4.3 cm (1.69 in.) diameter
Compliance Level
Group 1
Class B
Class A
N/A
Electromagnetic Environment – Guidance
Model 9681 uses RF energy only for its internal
function. Therefore, its RF emissions are very low
and are not likely to cause any interference in nearby
electronic equipment.
3M™ Surgical Clipper Professional, Model 9681 is
suitable for use in all establishments, including
domestic establishments and those directly
connected to the public low‑voltage power
supply network that supplies buildings used for
domestic purposes.
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