HOBBS MEDICAL, INC.

Address:8 Spring St,Stafford Springs,CT,06076,US

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Device Description : Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : A sterile non-bioabsorbable tubular device intended to be implanted in an obstru A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed pancreatic duct (e.g., due to stricture or malignancy) to maintain luminal patency; it may also be intended to treat a wide variety of conditions in pancreatic endoscopy (e.g., drain pseudocyst, treat fistula or duct disruption). It is made entirely of a synthetic polymer and has a continuous tube design with or without retention flanges. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : A sterile non-bioabsorbable tubular device intended to be implanted in an obstru A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed pancreatic duct (e.g., due to stricture or malignancy) to maintain luminal patency; it may also be intended to treat a wide variety of conditions in pancreatic endoscopy (e.g., drain pseudocyst, treat fistula or duct disruption). It is made entirely of a synthetic polymer and has a continuous tube design with or without retention flanges. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : A sterile non-bioabsorbable tubular device intended to be implanted in an obstru A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed pancreatic duct (e.g., due to stricture or malignancy) to maintain luminal patency; it may also be intended to treat a wide variety of conditions in pancreatic endoscopy (e.g., drain pseudocyst, treat fistula or duct disruption). It is made entirely of a synthetic polymer and has a continuous tube design with or without retention flanges. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1

Device Description : A sterile non-bioabsorbable tubular device intended to be implanted in an obstru A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed pancreatic duct (e.g., due to stricture or malignancy) to maintain luminal patency; it may also be intended to treat a wide variety of conditions in pancreatic endoscopy (e.g., drain pseudocyst, treat fistula or duct disruption). It is made entirely of a synthetic polymer and has a continuous tube design with or without retention flanges. This is a single-use device.

Device Class : 2

Duns Number: 076769355

Premarket Exempt : No

Product Code : FGE

Prescription Use : Yes

Device Count : 1