Speculum

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name: SPECULUM FDA UDI
Generic Name: Nasal speculum, reusable FDA UDI
Device Name: PITUITARY, CUSHING LANDOLT, 110 X 15 MM BLADE FDA UDI
Model / Reference: 24-999-11-07 FDA UDI
Description: PITUITARY, CUSHING LANDOLT, 110 X 15 MM BLADE FDA UDI

Identifiers

Primary DI / UDI-DI: 00888118034694 FDA UDI
FDA Product Code: EPY FDA UDI
GMDN Term: Nasal speculum, reusable 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Nasal speculum, reusable

Speculum by KLS-Martin L.P. — 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: KLS-Martin L.P.

Sources (1)

FDA UDI 1c309a63-e161-44dc-86c8-28e82fa7ff8b 34 fields · synced May 30, 2026