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Crédits
Devices
Device Recall Microcuff
Modèle / numéro de série
Product code 35111-07, 35112-07, 35113-07 and 35114-07, All Lots.
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide, including USA, Canada, Europe, Australia, Chile, Hong Kong, Singapore, Thailand, India, Malaysia and Saudi Arabia.
Description du dispositif
Kimberly-Clark Microcuff Endotracheal Tube, Pediatric Oral/Nasal Magill, sizes 3.0mm, 3.5mm, 4.0mm, and 4.5mm, Rx Only, Sterile, Manufacturer: Kimberly-Clark NV Belgicastraat 13, 1930 Zaventem, Belgium, Made in Malaysia
Manufacturer
Kimberly-Clark Corporation
1 Event
Rappel de Device Recall Microcuff
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Fabricant
Kimberly-Clark Corporation
Adresse du fabricant
Kimberly-Clark Corporation, 1400 Holcomb Bridge Rd, Roswell GA 30076
Source
USFDA
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Device Recall Microcuff
Modèle / numéro de série
All lots of the product manufactured are being recalled
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
U.S.
Description du dispositif
Microcuff Pediatric Endotracheal Tubes - Oral Pre-Curved: || ID Size: 3,0mm, Microcuff Product Reference: I-MPEDC-30; || ID Size: 3,5mm, Product Reference: I-MPEOC-35; || ID Size: 4,0mm, Product Reference: I-MPEOC-40; || ID Size: 4.5mm, Product Reference: I-MPEOC-45; || ID Size: 5,0mm, Product Reference: I-MPEOC-50; || ID Size: 5,5mm, Product Reference: I-MPEOC-55; || ID Size: 6,0mm, Product Reference: I-MPEOC-60; || ID Size: 6,5mm, Product Reference: I-MPEOC-65 and || ID Size: 7,0mm, Product Reference: I-MPEOC-70 * Sterile * Single use only * Manufactured by Euromedical Industries, Sdn. Bhd., Bakar Arang Industrial Estate, 08000 Sungai Patani, Kedah, Malaysia * Distributed by: Microcuff GmbH, Hohnerweg 2-4, D-69469 Weinheim, Germany.
Manufacturer
Microcuff Gmbh
Device Recall Microcuff
Modèle / numéro de série
All lots of the product manufactured are being recalled.
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
U.S.
Description du dispositif
Microcuff Adult Endotracheal Tubes - Oral/Nasal Magill with Murphy Eye * || ID Size: 5,0mm, Microcuff Product Reference: I-HMICU-50; || ID Size: 5.5mm, Product Reference: I-HMICU- 55; || ID Size: 6.0mm, Product Reference: I-HMICU- 60; || ID Size: 6.5mm, Product Reference: I-HMICU- 65; || ID Size: 7.0mm, Product Reference: I-HMICU- 70; || ID Size: 7.5mm, Product Reference: I-HMICU-75; || ID Size: 8.0mm, Product Reference: I-HMICU-80; || ID Size: 8.5mm, Product Reference: I-HMICU-85; || ID Size: 9.0mm, Product Reference: I-HMICU-90; || and ID Size: 10.0mm Product Reference: I-HMICU-10 * Sterile * Single use only * Manufactured by Euromedical Industries, Sdn. Bhd., Bakar Arang Industrial Estate, 08000 Sungai Patani, Kedah, Malaysia * Distributed by: Microcuff GmbH, Hohnerweg 2-4, D-69469 Weinheim, Germany.
Manufacturer
Microcuff Gmbh
Device Recall Microcuff
Modèle / numéro de série
Product code: 35162-07, 35162-07, 35163-07 and 35164-07, All lot numbers
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide, including USA, Canada, Europe, Australia, Chile, Hong Kong, Singapore, Thailand, India, Malaysia and Saudi Arabia.
Description du dispositif
Kimberly Clark Microcuff Endotracheal Tube, Pediatric Oral Curved, sizes 3.0mm, 3.5mm, 4.0mm and 4.5mm, Rx Only, Sterile, Manufacturer: Kimberly-Clark NV Belgicastraat 13, 1930 Zaventem, Belgium, Made in Malaysia
Manufacturer
Kimberly-Clark Corporation
Language
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