Reprocessed QuickPass SutureLasso, 90 Deg, w/out Nitinol Wire

FDA UDI

Class I (US FDA UDI)

by Suretek Medical

Identity

Trade Name: Reprocessed QuickPass SutureLasso, 90 Deg, w/out Nitinol Wire FDA UDI
Generic Name: Suturing unit, reprocessed FDA UDI
Model / Reference: AR-6068-90-X FDA UDI

Identifiers

Primary DI / UDI-DI: B390AR606890X1 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Suturing unit, reprocessed FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Suturing unit, reprocessed

Reprocessed QuickPass SutureLasso, 90 Deg, w/out Nitinol Wire by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Suretek Medical

Sources (1)

FDA UDI 896c5111-07e3-4f51-8084-7130744057a7 32 fields · synced Jun 6, 2026