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Sources: EU EUDAMED, US FDA
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FDA UDI
TELEFLEX INCORPORATED·10801902217346·One-Lumen CVC
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FDA UDI
TELEFLEX INCORPORATED·10801902104660·Central Venous Catheterization Set with Blue Fl...
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TELEFLEX INCORPORATED·00801902104595·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·00801902000828·Radial Artery Catheterization Kit
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FDA UDI
TELEFLEX INCORPORATED·10801902121131·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·10801902104653·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·10801902104592·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·10801902121124·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·00801902104663·Central Venous Catheterization Set with Blue Fl...
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TELEFLEX INCORPORATED·10801902121186·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·00801902000781·Radial Artery Catheterization Kit
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FDA UDI
TELEFLEX INCORPORATED·00801902000774·Radial Artery Catheterization Kit
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FDA UDI
TELEFLEX INCORPORATED·00801902104625·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·10801902121179·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·10801902104622·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·00801902104656·Central Venous Catheterization Set with Blue Fl...
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FDA UDI
TELEFLEX INCORPORATED·00801902000811·Radial Artery Catheterization Kit
Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray DS USA Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 This is a device used to administer to a patient continuously or intermittently a general inhalation anesthetic and to maintain a patient's ventilation.
FDA Enforcement
Class I
·Terminated·Mindray DS USA, Inc. d.b.a. Mindray North America·November 28, 2012
UNKNOWN EEA
FDA Adverse Event
Injury
·US SURGICAL PUERTO RICO·Product code GDW·June 29, 2021
ENDOPATH*STEALTH CIR STAPLER (EXACT CODE UNKNOWN)
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·June 13, 2025