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AEROECLIPSE II Breath Actuated Nebulizer without Oxygen Tubing

FDA UDI

Class II (US FDA UDI)

by Trudell Medical International

Identity

Trade Name
AEROECLIPSE II Breath Actuated Nebulizer without Oxygen Tubing FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
AEROECLIPSE II Breath Actuated Nebulizer without Oxygen Tubing FDA UDI
Model / Reference
105542 FDA UDI
Description
AEROECLIPSE II Breath Actuated Nebulizer without Oxygen Tubing FDA UDI

Identifiers

Primary DI / UDI-DI
00762860055421 FDA UDI
510(k) Number
K053605 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nebulizing system delivery set, reusable

AEROECLIPSE II Breath Actuated Nebulizer without Oxygen Tubing by Trudell Medical International — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Nebulizing system delivery set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e8912418-27a6-4ac7-89bb-5988484d7644 35 fields · synced Jun 8, 2026