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Polytech Noseclip

FDA UDI

Class I (US FDA UDI)

by Polytechnic Resources, Inc.

Identity

Trade Name
Polytech Noseclip FDA UDI
Generic Name
Nose clip, single-use FDA UDI
Device Name
A device intended to be used to compress the nose externally, to ensure that airflow is exclusively conducted through the mouth during examinations of the pulmonary function (e.g., spirometry), and/or to stop nosebleeds (epistaxis). It is typically constructed of plastic with rubber or foam tips. This is a single-use device. FDA UDI
Model / Reference
N100753S FDA UDI
Description
A device intended to be used to compress the nose externally, to ensure that airflow is exclusively conducted through the mouth during examinations of the pulmonary function (e.g., spirometry), and/or to stop nosebleeds (epistaxis). It is typically constructed of plastic with rubber or foam tips. This is a single-use device. FDA UDI

Identifiers

Primary DI / UDI-DI
B446N100753S1 FDA UDI
FDA Product Code
BXJ FDA UDI
GMDN Term
Nose clip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6225 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nose clip, single-use

Polytech Noseclip by Polytechnic Resources, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nose clip, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 43230cd6-5d0e-4d32-9482-ed94afa20aa0 33 fields · synced Jun 8, 2026