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Crédits
Devices
Device Recall Overpressure Safety Valve
Modèle / numéro de série
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide distribution: US, Canada, Colombia, UK, Belgium, and Japan
Description du dispositif
Custom surgical kits containing TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 and (b) LH130J || Catalog numbers: || US distribution: || LH130 || 74369 || 71156 || 71551-02 || 71413 || 71692 || 74102 || 75490 || 74432-01 || 75477 || 75478 || 75104-02 || 75104-03 || 75477-01 || 75037 || 75973 || 75308-01 || 75688 || 70571-06 || 75114-01 || 72755 || 73306 || 71180-01 || 73307 || 75163 || 75164 || 75787 || 75163-01 || 73055-02 || 75450 || 75451 || 75452 || 75453 || 75453-01 || 75999 || 75451-01 || 72481-01 || 75197 || 73968 || 75416 || 73648 || 71519-02 || 71801-01 || 72846 || 74163-02 || 74178-03 || 74986 || 75607 || 74162-01 || 74163-03 || 73454-01 || 71296-01 || 74924 || 73344-04 || 73500-04 || 74924-01 || 73143-02 || 76393 || 74248-01 || 73820-01 || 75261 || 75594 || 74022-01 || 66001-01 || 66004-01 || 74916 || 72736-02 || B72736-02 || 70815 || 70815-01 || 70815-02 || 74356-02 || 73208-03 || 73001-02 || 73957-01 || 74460-01 || 70089-06 || 75168 || 75171 || 75240 || 74382-01 || 66467 || 70089-07 || 74965-03 || 75168-01 || 75240-01 || 66467-01 || 70089-08 || 73177 || 76006 || 73177-01 || 76038 || 75252-01 || 76316 || 75805-02 || 73346 || 76414 || 75790 || 75678 || 62007-01 || 66229 || 75075 || 62007-02 || 65382 || 75788 || 75788-01 || 70533-10 || 75936 || 75936-01 || 63123 || 72241 || 70148-02 || 70730 || 70772 || 74732 || 75090 || 75090-01 || 75090-02 || 75089-01 || 73468 || 74430 || 74921-02 || 75881 || 64523-02 || 64619-02 || 64522-03 || 64521-02 || 65560-03 || 64912-04 || 65560-04 || 71064 || 65570 || 71062-01 || 71061-02 || 71060-01 || 71962-04 || 71965-04 || 75948 || 71962-05 || 74401-01 || 74400-01 || 74399-02 || 75944 || 759
Manufacturer
Terumo Cardiovascular Systems Corporation
1 Event
Rappel de Device Recall Overpressure Safety Valve
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Fabricant
Terumo Cardiovascular Systems Corporation
Adresse du fabricant
Terumo Cardiovascular Systems Corporation, 125 Blue Ball Rd, Elkton MD 21921-5315
Société-mère du fabricant (2017)
Terumo Corp.
Source
USFDA
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Device Recall Overpressure Safety Valve
Modèle / numéro de série
SAFETY ALERT Lot Codes: (a) RH14, RK11, RK20, RL02, RM06, RM20, RN10, RP08, TD16, TE13, TE27, TF14, TF21, TG04, TG11, TG17, TH06, TH16, TK10, TK24, TL08, TL21, TM28, TP14, UA11, UA18, UA25, UC08, UC22, UD14, UD21, UD28, UE05, UE18, UF09, UG06, UK01, UL12, UM10, UM31, UP05, VA02, VC06, VD06, VE10 (b) RH14, RH21, RK18, RL15, RM01, RM22, RN24, RP01, TA19, TF05, TF27, TG19, TH20, TK24, TL01, TM12, TN09, TP03, UA20, UC15, UD22, UE04, UE18, UF02, UG13, UH11, UK15, UL06, UM10, VA02, VA30, VC27, VE03, VF01 LH130 PRODUCT CORRECTION lot codes or serial number range: TA19 through VD06, distribution date range: 08Apr2015 through 20Jan2017
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide distribution: US, Canada, Colombia, UK, Belgium, and Japan
Description du dispositif
TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 (b) LH130J
Manufacturer
Terumo Cardiovascular Systems Corporation
Language
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