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SECQURE Ultimate

FDA UDI

Class II (US FDA UDI)

by Secqure Surgical, Corp.

Identity

Trade Name
SECQURE Ultimate FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Suction / Irrigation Set with Single Spike FDA UDI
Model / Reference
CQ3851ULT FDA UDI
Description
Suction / Irrigation Set with Single Spike FDA UDI

Identifiers

Primary DI / UDI-DI
00863634000491 FDA UDI
510(k) Number
K081398 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

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

Category: Surgical irrigation/aspiration tubing set

SECQURE Ultimate by Secqure Surgical, Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e1280338-8326-44b0-8ba3-c5ec0d98cb73 34 fields · synced Jun 1, 2026