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Hayden Medical

FDA UDI

Class II (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name
Hayden Medical FDA UDI
Generic Name
Endoscopic surgical probe FDA UDI
Device Name
Laparoscopic Tactile Probe 5mm, graduated, 45cm working length FDA UDI
Model / Reference
HE10-1110-45 FDA UDI
Description
Laparoscopic Tactile Probe 5mm, graduated, 45cm working length FDA UDI

Identifiers

Catalog Number
HE10-1110-45 FDA UDI
Primary DI / UDI-DI
00840319752524 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic surgical probe 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

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: Endoscopic surgical probe

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

Similar devices

Also classified as Endoscopic surgical probe.

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 99067fd0-1077-4d2d-b55d-8ca06a59cb9b 35 fields · synced May 30, 2026