← Back to catalogue

Nasal speculum, chrome plated

FDA UDI

Class I (US FDA UDI)

by Rudolf Riester GmbH & Co. KG

Identity

Trade Name
Nasal speculum, chrome plated FDA UDI
Generic Name
Nasal speculum, reusable FDA UDI
Device Name
The nasal speculum is produced for illumination and therefore examination of the inside of the nose. FDA UDI
Model / Reference
10440 FDA UDI
Description
The nasal speculum is produced for illumination and therefore examination of the inside of the nose. FDA UDI

Identifiers

Catalog Number
10440 FDA UDI
Primary DI / UDI-DI
04045396010291 FDA UDI
510(k) Number
K925754 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal speculum, reusable

Nasal speculum, chrome plated by Rudolf Riester GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal speculum, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d5898b97-ad9d-49ba-99ec-f7dfd610887f 35 fields · synced May 30, 2026