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Aero®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
AERO® FDA UDI
Generic Name
Polymeric tracheal/bronchial stent, non-bioabsorbable FDA UDI
Model / Reference
00884450030783 FDA UDI

Identifiers

Catalog Number
90129-204/C FDA UDI
Primary DI / UDI-DI
00884450030783 FDA UDI
FDA Product Code
JCT FDA UDI
GMDN Term
Polymeric tracheal/bronchial stent, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Polymeric tracheal/bronchial stent, non-bioabsorbable

Aero® is a non-bioabsorbable, polymeric tracheal/bronchial stent designed to maintain luminal patency in patients with tracheal and/or bronchial obstructions, fistulae, tumors, scarring, surgical resection, and anastomosis. Made entirely of synthetic polymer(s), it is available for implantation, often as part of a comprehensive treatment plan.

Similar devices

Also classified as Polymeric tracheal/bronchial stent, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI cc72efd9-dfc2-4ef1-ad77-405f26a6d63c 34 fields · synced Jul 27, 2026