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Regard™

FDA UDI

Class II (US FDA UDI)

by Resource Optimization & Innovation, L.l.c.

Identity

Trade Name
Regard™ FDA UDI
Generic Name
Vascular access device flush/disinfection tool FDA UDI
Model / Reference
303394 FDA UDI

Identifiers

Primary DI / UDI-DI
20326053105160 FDA UDI
FDA Product Code
OFF FDA UDI
GMDN Term
Vascular access device flush/disinfection tool FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1140 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Vascular access device flush/disinfection tool

Regard™ by Resource Optimization & Innovation, L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular access device flush/disinfection tool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0aeda504-b0f3-4020-8413-359ce666eb31 32 fields · synced May 30, 2026