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Angel Catheter

FDA UDI

Class II (US FDA UDI)

by Mermaid Medical A/S

Identity

Trade Name
Angel Catheter FDA UDI
Generic Name
Vena cava filter, temporary/permanent FDA UDI
Device Name
SHORT-TERM INTRAVASCULAR FILTER CATHETER FDA UDI
Model / Reference
AC3930A FDA UDI
Description
SHORT-TERM INTRAVASCULAR FILTER CATHETER FDA UDI

Identifiers

Primary DI / UDI-DI
15711055005002 FDA UDI
510(k) Number
K160747 FDA UDI
FDA Product Code
PNS FDA UDI
GMDN Term
Vena cava filter, temporary/permanent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3375 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

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: Vena cava filter, temporary/permanent

Angel Catheter by Mermaid Medical A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vena cava filter, temporary/permanent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mermaid Medical A/S

Sources (1)

  • FDA UDI f34280b3-db7e-4da0-8164-59bbc2990ca6 34 fields · synced May 30, 2026