CFM Technologies

FDA UDI

Class I (US FDA UDI)

by C F M Technologies Inc

Identity

Trade Name: CFM Technologies FDA UDI
Generic Name: Direct ophthalmoscope FDA UDI
Device Name: Deluxe ENT Field Corpsman Kit. This kit contains a versatile set of components designed to facilitate effective examination of the eyes, ears, nose and throat. FDA UDI
Model / Reference: ENT-DMK FDA UDI
Description: Deluxe ENT Field Corpsman Kit. This kit contains a versatile set of components designed to facilitate effective examination of the eyes, ears, nose and throat. FDA UDI

Identifiers

Primary DI / UDI-DI: 00850013958252 FDA UDI
FDA Product Code: HPN FDA UDI
JYG FDA UDI
ERA FDA UDI
GMDN Term: Direct ophthalmoscope FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4445 FDA UDI
874.4420 FDA UDI
874.4770 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

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Ear speculum, reusable Ophthalmic/otologic diagnostic set Otoscope, direct Direct ophthalmoscope

CFM Technologies by C F M Technologies Inc — 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: C F M Technologies Inc

Sources (1)

FDA UDI def3afad-f4d3-4842-a597-270dff67f976 34 fields · synced May 31, 2026