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Aero Dv®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

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

Identifiers

Catalog Number
90129-305 FDA UDI
Primary DI / UDI-DI
00884450690796 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 DV is a highly effective, non-bioabsorbable tubular device intended to maintain luminal patency in various medical conditions. Designed for implantation into the trachea or bronchus/bronchiole, it is made from synthetic polymer(s) and may feature expandable designs, disposable options, and self-expanding capabilities.

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 dfdb9a2d-73f7-47cc-a234-a3d9f2e2cd66 34 fields · synced Oct 6, 2026