94 results
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83ms
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Sources: EU EUDAMED, US FDA
TECH MEDICAL SERVICES, INC.
FDA registration
TECH MEDICAL SERVICES, INC.·10 products·🇺🇸 United States
1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", sterile; 4. UNIMAX Detachable endo pocket, REF FEP936116, 3" x 6", sterile; 5. UNIMAX Detachable endo pocket, REF FEP979000, 8" x 10", sterile; 6. ConMed Corporation Detachable endo pocket, REF SB936, 3" x 6", sterile; 7. ConMed Corporation Detachable endo pocket, REF SB957, 5" x 7", sterile; 8. ConMed Corporation Detachable endo pocket, REF SB979, 7.5" x 9", sterile; 9. ConMed Corporation Detachable endo pocket, REF SB979-CA, 7.5 x 9", sterile; 10. ConMed Corporation Detachable endo pocket, REF SB936-CA, 3" x 6", sterile;
FDA Enforcement
Class II
·Ongoing·UNIMAX MEDICAL SYSTEMS INC·September 25, 2024
GAMMA PROBE COVER
FDA Adverse Event
Malfunction
·TECH MEDICAL SERVICES, INC.·Product code IZD·October 15, 2009
TECH MEDICAL SERVICE ENDO RETRIEVAL POUCH
FDA Adverse Event
Malfunction
·TECH MEDICAL SERVICES, INC.·Product code GCJ·February 3, 2022
1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", sterile; 4. UNIMAX Detachable endo pocket, REF FEP936116, 3" x 6", sterile; 5. UNIMAX Detachable endo pocket, REF FEP979000, 8" x 10", sterile; 6. ConMed Corporation Detachable endo pocket, REF SB936, 3" x 6", sterile; 7. ConMed Corporation Detachable endo pocket, REF SB957, 5" x 7", sterile; 8. ConMed Corporation Detachable endo pocket, REF SB979, 7.5" x 9", sterile; 9. ConMed Corporation Detachable endo pocket, REF SB979-CA, 7.5 x 9", sterile; 10. ConMed Corporation Detachable endo pocket, REF SB936-CA, 3" x 6", sterile;
FDA Recall
Open, Classified
·UNIMAX MEDICAL SYSTEMS INC 8F-2, NO·Product code GCJ·June 25, 2024
COMPANION 5
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·July 14, 2022
ECLIPSE 5
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·June 4, 2020
SYNCHRON LXI 725 CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·November 4, 2011
ECLIPSE 5
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·May 28, 2020
ECLIPSE 5
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·June 4, 2020
ECLIPSE 5
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·June 11, 2020
O-ARM 1000 IMAGING SYSTEM 3RD EDITION
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 28, 2016
FREESTYLE COMFORT
FDA Adverse Event
Malfunction
·CAIRE INC.·Product code CAW·September 1, 2022
COULTER AC T 5 DIFF AUTOLOADER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·February 7, 2012
MAXI MOVE (AHE)
FDA Adverse Event
Other
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·November 12, 2010
SARA 2000
FDA Adverse Event
Injury
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·November 19, 2010
ALM
FDA Adverse Event
Other
·MAQUET S.A.·Product code FSY·December 23, 2009
COLLEAGUE CXE VOLUMETRICINFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 9, 2010
DAVINCI XI
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC·Product code NAY·February 7, 2024
PARKER BATH
FDA Adverse Event
Other
·ARJO HOSPITAL EQUIPMENT AB·Product code ILJ·October 14, 2010