← Back to catalogue

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
00884450625309 FDA UDI

Identifiers

Catalog Number
90129-208/D FDA UDI
Primary DI / UDI-DI
00884450625309 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Polymeric tracheal/bronchial stent, non-bioabsorbable

Aero\® is a highly effective and versatile non-bioabsorbable tracheal/bronchial stent designed to maintain luminal patency in patients with various obstructive or stenotic conditions. Made entirely of synthetic polymer(s), this implantable device provides long-term support and relief, making it an ideal solution for complex cases. With its expandable design and disposable features, Aero\® offers flexibility and convenience in clinical settings.

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI eb4755e6-f962-4477-8991-0dc10eb53147 34 fields · synced Jul 24, 2026