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Clear Sequence

FDA UDI

Class II (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Clear Sequence FDA UDI
Generic Name
Vascular catheterization support/maintenance kit, non-medicated FDA UDI
Model / Reference
83592 FDA UDI

Identifiers

Primary DI / UDI-DI
10809160398920 FDA UDI
FDA Product Code
PEZ FDA UDI
GMDN Term
Vascular catheterization support/maintenance kit, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Vascular catheterization support/maintenance kit, non-medicated

Clear Sequence by Medical Action Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheterization support/maintenance kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Action Industries Inc.

Sources (1)

  • FDA UDI 34b00671-ee53-49b3-8bfe-62737a36b1dc 33 fields · synced May 31, 2026