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Aspira®

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Aspira® FDA UDI
Generic Name
Pleural/peritoneal drainage catheterization kit FDA UDI
Model / Reference
00884450394922 FDA UDI

Identifiers

Catalog Number
4992507B/A FDA UDI
Primary DI / UDI-DI
00884450394922 FDA UDI
FDA Product Code
DWM FDA UDI
GMDN Term
Pleural/peritoneal drainage catheterization kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Category: Pleural/peritoneal drainage catheterization kit

Aspira is a unique and innovative pleural/peritoneal drainage catheterization kit designed for patients requiring temporary drainage of excess fluid from the lungs or abdomen. As part of your ongoing care, it helps alleviate symptoms such as congestion, discomfort, and swelling, allowing you to recover more quickly.

Similar devices

Also classified as Pleural/peritoneal drainage catheterization kit.

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 8a82934e-2266-462d-8a47-81feb4e0d397 33 fields · synced Jul 19, 2026