Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name: JEDMED FDA UDI
Generic Name: Ear speculum, single-use FDA UDI
Device Name: SPECULUM SEPTUM 64MM BLADES FDA UDI
Model / Reference: 52-2182 FDA UDI
Description: SPECULUM SEPTUM 64MM BLADES FDA UDI

Identifiers

Catalog Number: 52-2182 FDA UDI
Primary DI / UDI-DI: M6335221820 FDA UDI
FDA Product Code: EPY FDA UDI
GMDN Term: Ear speculum, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.1800 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Ear speculum, single-use

Jedmed by JEDMED Instrument Company — 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: JEDMED Instrument Company

Sources (1)

FDA UDI d07042d7-e72a-427a-ae64-8ad652a74e17 34 fields · synced May 30, 2026