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Aspirator

FDA UDI

Class II (US FDA UDI)

by Vitalograph Ireland, Ltd.

Identity

Trade Name
Aspirator FDA UDI
Generic Name
Emergency airway clearance suction system, manual FDA UDI
Device Name
2510 EMERGENCY ASPIRATOR(1) FDA UDI
Model / Reference
2510 FDA UDI
Description
2510 EMERGENCY ASPIRATOR(1) FDA UDI

Identifiers

Primary DI / UDI-DI
15099169251004 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
Emergency airway clearance suction system, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Emergency airway clearance suction system, manual

Aspirator by Vitalograph Ireland, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction system, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vitalograph Ireland, Ltd.

Sources (1)

  • FDA UDI 2a2bf9e7-c6c1-46ba-88b6-588b7232b56c 34 fields · synced May 31, 2026