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Elmed Incorporated

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED INCORPORATED FDA UDI
Generic Name
Obstetrical forceps, reusable FDA UDI
Device Name
Simpson Obstetrical Forceps, Overall Length 14” FDA UDI
Model / Reference
ST515300 FDA UDI
Description
Simpson Obstetrical Forceps, Overall Length 14” FDA UDI

Identifiers

Catalog Number
ST515300 FDA UDI
Primary DI / UDI-DI
00198506017568 FDA UDI
FDA Product Code
HCZ FDA UDI
GMDN Term
Obstetrical forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Obstetrical forceps, reusable

Elmed Incorporated by Elmed Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Obstetrical forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI f4316b49-b162-4b67-8811-0364d32eff98 35 fields · synced May 31, 2026