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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
Open-surgery biopsy forceps, reusable FDA UDI
Device Name
Biopsy and Grasping Forceps, delicate pattern, 1,5mm shaft, double action, 5-1/2" (14 cm) working length, 3mm oval cup FDA UDI
Model / Reference
200-130 FDA UDI
Description
Biopsy and Grasping Forceps, delicate pattern, 1,5mm shaft, double action, 5-1/2" (14 cm) working length, 3mm oval cup FDA UDI

Identifiers

Catalog Number
200-130 FDA UDI
Primary DI / UDI-DI
00840319742334 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Open-surgery biopsy forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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: Open-surgery biopsy forceps, reusable

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

Similar devices

Also classified as Open-surgery biopsy forceps, reusable.

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 861e247a-e2a2-4d89-a5ef-6ab52dc060e3 35 fields · synced May 30, 2026