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Noseclip

FDA UDI

Class I (US FDA UDI)

by Vitalograph Ireland, Ltd.

Identity

Trade Name
Noseclip FDA UDI
Generic Name
Nose clip, single-use FDA UDI
Device Name
2030 NOSE CLIPS FDA UDI
Model / Reference
2030 FDA UDI
Description
2030 NOSE CLIPS FDA UDI

Identifiers

Primary DI / UDI-DI
15099169202327 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nose clip, single-use

Noseclip by Vitalograph Ireland, Ltd. — 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 b67871da-fa1e-4f00-a966-7cd65b912863 34 fields · synced Jun 8, 2026