← Back to catalogue

Nasal Speculum

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
NASAL SPECULUM FDA UDI
Generic Name
Nasal speculum, single-use FDA UDI
Device Name
NASAL SPECULUM 5-1/2" FDA UDI
Model / Reference
NASAL SPECULUM FDA UDI
Description
NASAL SPECULUM 5-1/2" FDA UDI

Identifiers

Catalog Number
NSP500 FDA UDI
Primary DI / UDI-DI
B974NSP5000 FDA UDI
FDA Product Code
EPY FDA UDI
GMDN Term
Nasal 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

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 5.5 Inch FDA UDI

Category: Nasal speculum, single-use

Nasal Speculum by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal speculum, single-use.

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

Manufacturer
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI 60371187-dbfb-45e3-95ec-e2e07ecc3760 35 fields · synced May 30, 2026