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Medivators Hookup

FDA UDI

Class II (US FDA UDI)

by Medivators Inc.

Identity

Trade Name
Medivators Hookup FDA UDI
Generic Name
Luminal device flushing tubing set, reusable FDA UDI
Device Name
Hookup, OAI Leak Tester connects MEDIVATORS reprocessing equipment to endoscopes or related accessories. FDA UDI
Model / Reference
Hookup FDA UDI
Description
Hookup, OAI Leak Tester connects MEDIVATORS reprocessing equipment to endoscopes or related accessories. FDA UDI

Identifiers

Catalog Number
DSD110HU0102 FDA UDI
Primary DI / UDI-DI
00677964085345 FDA UDI
510(k) Number
K092387 FDA UDI
K914145 FDA UDI
FDA Product Code
FEB FDA UDI
GMDN Term
Luminal device flushing tubing set, 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

No

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

Yes

FDA UDI

Category: Luminal device flushing tubing set, reusable

Medivators Hookup by Medivators Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luminal device flushing tubing set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medivators Inc.

Sources (1)

  • FDA UDI 6cc688e4-eb79-49c7-b68d-6ec708393f7f 36 fields · synced Jun 1, 2026