Fluid Dock

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name: Fluid Dock FDA UDI
Generic Name: General-purpose catheter connector, sterile FDA UDI
Device Name: Filling Device FDA UDI
Model / Reference: M00499150 FDA UDI
Description: Filling Device FDA UDI

Identifiers

Primary DI / UDI-DI: 08714729745167 FDA UDI
FDA Product Code: OBJ FDA UDI
GMDN Term: General-purpose catheter connector, sterile FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: General-purpose catheter connector, sterile

Fluid Dock by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Boston Scientific

Sources (1)

FDA UDI 79928836-b3b5-4815-8c47-4de5d113d177 33 fields · synced May 30, 2026