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Heartline Flushing Adapter

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEARTLINE FLUSHING ADAPTER FDA UDI
Generic Name
Endoscope flushing adaptor, reusable FDA UDI
Device Name
HEARTLINE FLUSHING ADAPTER (LUER) FDA UDI
Model / Reference
2800-005 FDA UDI
Description
HEARTLINE FLUSHING ADAPTER (LUER) FDA UDI

Identifiers

Catalog Number
2800-005 FDA UDI
Primary DI / UDI-DI
00192896006744 FDA UDI
510(k) Number
K152400 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscope flushing adaptor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope flushing adaptor, reusable

Heartline Flushing Adapter by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope flushing adaptor, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b1e4c681-b625-4544-9d08-9852f79eea50 36 fields · synced Jun 1, 2026