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Hayden Medical

FDA UDI

Class I (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name
Hayden Medical FDA UDI
Generic Name
Dissection board FDA UDI
Device Name
Cartilage Cutting Block for thicknesses of 0.5mm-2.0mm, 5mmx55mmx10mm, delrin FDA UDI
Model / Reference
194-410 FDA UDI
Description
Cartilage Cutting Block for thicknesses of 0.5mm-2.0mm, 5mmx55mmx10mm, delrin FDA UDI

Identifiers

Primary DI / UDI-DI
00840319753132 FDA UDI
FDA Product Code
NNR FDA UDI
GMDN Term
Dissection board FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dissection board

Hayden Medical by Hayden Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dissection board.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hayden Medical Inc

Sources (1)

  • FDA UDI 3242b98d-99d0-4f98-8606-44eb3ef32d03 34 fields · synced May 31, 2026