Products

Blanket Warmer IFbw

The Memmert blanket warmer IFbw is a Class I medical device.

Blanket Warmer IFbw Class I medical device IF260bw 824 x 1183 x 684 mm
Classified medical device

Immediately ready-to-hand and precisely preheated blankets
Blanket Warmer IFbw

Blanket warmers are vital when attending to seriously injured patients, especially in emergency rooms, as well as in delivery rooms or recovery rooms, where they are useful on a daily basis. In a blanket warmer IFbw, blankets and cloths are preheated to a precise temperature. It is essential for keeping patients warm. This minimises the risk of complications such as wound infections, cardiovascular disorders, cardiac arrhythmia or vascular disorders.
  • Temperature range up to +80 °C
  • 4 model sizes (with a chamber volume of 108 to 749 litres)
  • Forced air circulation F, fixed at 100%

The blanket warmer IFbw provides outstanding safety

The Memmert blanket warmer IFbw has an impressive range of safety features:
1.The heating capacity is limited to 80 ℃ to prevent cotton textiles from overheating if the blanket warmer is overloaded
2.Three platinum sensors monitor the surface temperatures in the hermetically sealed interior where the air is constantly circulated
3. An automatic open door sensor switches the heater and fan off if the door is opened
4. A mechanical temperature limiter interrupts the power supply at a maximum temperature of 85 ℃

Intended use of the IFbw as a medical device

Memmert blanket warmers IFbw are Class I medical devices. Memmert is bringing medical devices of class I according to the regulation MDR (EU) 2017/745 into circulation. According to the intended purpose, Memmert blanket warmers IFbw are suitable for warming non-sterile blankets and cloths.

A Memmert blanket warmer offers unique advantages

  • intuitive and easy-to-use operating concept
  • almost exclusive use of high-quality, corrosion-resistant and easily cleanable stainless steel for the working chamber and housing
  • heating concept specifically adapted for a precise and homogenous temperature control
  • a wide range of options for reading the data logging using interfaces, integrated data logger and Software AtmoCONTROL
  • 3 years guarantee worldwide

Standard units are safety-approved and bear the test marks

VDE
CE
UL

Intended use as medical device

Memmert is bringing medical devices of class I according to EU Directive (EU) 2017/745 into circulation.

Type Intended use as medical device Classification according to (EU) 2017/745
UNmplus, UFmplus The appliance may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. I
UNm, UFm, INm, IFm The appliance may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. I
INmplus, IFmplus Im may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. Implus may be used for temperature control of rinsing and infusion solutions and contrast agents. I
IFbw The appliance is used to heat non-sterile cloths and covers. Any other use is improper
and may cause damage or danger.
I

Memmert is bringing medical devices of class IIa and IIb into circulation according to MDD 93/42/EEC until 31.12.2028 according to the transitional provisions (EU) 2023/607 by the (EU) 2017/745 article 120 (2).

Type Intended use as medical device Classification according to 93/42/EWG
SNplus, SFplus The product is intended for the sterilisation of medical devices with dry heat at atmospheric pressure. IIb
SN, SF The product is intended for the sterilisation of medical devices with dry heat at atmospheric pressure. IIb
ICOmed The CO2 incubator ICOmed is used to generate and maintain constant ambient conditions for the in-vitro fertilisation (IVF) application field, especially for the incubation of oocytes, spermatozoa and zygotes in special culture dishes for IVF application as well as for gene expression and the biosynthesis of RNA and proteins. IIa

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Medical device consultant training

As part of our medical device consultant training, we qualify you in the consultation, use and instruction of our medical products, taking into account the currently applicable legal requirements with regard to the new Medical Devices Regulation (EU) 2017/745. We explain the requirements for dealers, the geographical scope as well as information on the reporting system and the tasks of a medical device consultant. After successful participation, you will receive a certificate of qualification as a medical device consultant for Memmert medical devices.

Have we piqued your interest? Please contact us at sales@memmert.com for more information.