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Princeton

FDA UDI

Class I (US FDA UDI)

by Princeton Medical Group, Inc.

Identity

Trade Name
PRINCETON FDA UDI
Generic Name
Nasal speculum, reusable FDA UDI
Device Name
NASAL SPECULUM COTTLE 50MM WITH LOCKING SCREW 5.5" FDA UDI
Model / Reference
47124-50S FDA UDI
Description
NASAL SPECULUM COTTLE 50MM WITH LOCKING SCREW 5.5" FDA UDI

Identifiers

Primary DI / UDI-DI
00810158215078 FDA UDI
FDA Product Code
HNW FDA UDI
GMDN Term
Nasal speculum, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Nasal speculum, reusable

Princeton by Princeton Medical Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal speculum, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2a5b3297-86cc-440c-a543-15672d02ae6a 33 fields · synced May 30, 2026