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DualCap®

FDA UDI

Class U (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
DualCap® FDA UDI
Generic Name
Luer-formatted disinfection cap FDA UDI
Model / Reference
10884450390730 FDA UDI

Identifiers

Catalog Number
500-LB/B FDA UDI
Primary DI / UDI-DI
10884450390730 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Luer-formatted disinfection cap FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer-formatted disinfection cap

DualCap® by Merit Medical Systems, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted disinfection cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 31ac8dcf-48c2-4993-9f86-538c6971e027 33 fields · synced Jun 9, 2026