Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name: ELMED FDA UDI
Generic Name: Hand-held surgical retractor, reusable FDA UDI
Device Name: GELPI PERINEAL RETRACTOR. SELF-RETAINING, SHARP TENACULUM PRONGS, TOTAL OPENING 3-1/4" (8.3CM). ARM LENGTH 4-3/4" (12.1CM). OL 7-1/4" (18.4CM) FDA UDI
Model / Reference: EL-GL500 FDA UDI
Description: GELPI PERINEAL RETRACTOR. SELF-RETAINING, SHARP TENACULUM PRONGS, TOTAL OPENING 3-1/4" (8.3CM). ARM LENGTH 4-3/4" (12.1CM). OL 7-1/4" (18.4CM) FDA UDI

Identifiers

Catalog Number: EL-GL500 FDA UDI
Primary DI / UDI-DI: 00842180171411 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Hand-held surgical retractor, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held surgical retractor, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Elmed Incorporated

Sources (1)

FDA UDI 751cf873-753f-4da0-a79d-88fbfa03b4ba 35 fields · synced Jun 6, 2026