← Back to catalogue

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
Schroeder Uterine Vulsellum Forceps 10" (25cm), curved on flat FDA UDI
Model / Reference
325-125 FDA UDI
Description
Schroeder Uterine Vulsellum Forceps 10" (25cm), curved on flat FDA UDI

Identifiers

Catalog Number
325-125 FDA UDI
Primary DI / UDI-DI
00840319749890 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Open-surgery biopsy forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Hayden Medical Inc

Sources (1)

  • FDA UDI b502853f-a1c2-4717-b343-fabb19daea02 35 fields · synced May 31, 2026