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HeartSpan®

FDA UDI

Class II (US FDA UDI)

by Merit Medical

Identity

Trade Name
HeartSpan® FDA UDI
Generic Name
Cardiac transseptal access set FDA UDI
Model / Reference
00884450198490 FDA UDI

Identifiers

Catalog Number
FST-085-01 FDA UDI
Primary DI / UDI-DI
00884450198490 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Cardiac transseptal access set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Cardiac transseptal access set

HeartSpan® by Merit Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac transseptal access set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical

Sources (1)

  • FDA UDI 7dfd9fbd-3eed-4c55-a0d7-b88da58b7937 34 fields · synced Jun 1, 2026