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Tenacore

FDA UDI

Class II (US FDA UDI)

by Tenacore Holdings, Inc.

Identity

Trade Name
Tenacore FDA UDI
Generic Name
Vacuum suction regulator/regulation set, general-purpose FDA UDI
Device Name
HP/Philips M1356A Ultrasound W/HORSESHOE AND KNOB FDA UDI
Model / Reference
TFCU-PH05-2303 FDA UDI
Description
HP/Philips M1356A Ultrasound W/HORSESHOE AND KNOB FDA UDI

Identifiers

Primary DI / UDI-DI
00852189007079 FDA UDI
510(k) Number
K043075 FDA UDI
FDA Product Code
HGM FDA UDI
GMDN Term
Vacuum suction regulator/regulation set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2740 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vacuum suction regulator/regulation set, general-purpose

Tenacore by Tenacore Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum suction regulator/regulation set, general-purpose.

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 a2a76061-ab11-4b41-8b85-07fab4c89803 34 fields · synced Jun 1, 2026