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Visu-Loc

FDA UDI

Class II (US FDA UDI)

by Microline Surgical, Inc.

Identity

Trade Name
Visu-Loc FDA UDI
Generic Name
Open-surgery ligation clip applier FDA UDI
Device Name
Visu-Loc 5mm Multi-Fire Spring Clip Applier, 20 clips, Disposable FDA UDI
Model / Reference
2001 FDA UDI
Description
Visu-Loc 5mm Multi-Fire Spring Clip Applier, 20 clips, Disposable FDA UDI

Identifiers

Catalog Number
2001 FDA UDI
Primary DI / UDI-DI
00811099010418 FDA UDI
FDA Product Code
FZP FDA UDI
GMDN Term
Open-surgery ligation clip applier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 FDA UDI
Commercial Distribution
Not 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

Visu-Loc by Microline Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d352d6c-fd3e-4b0c-ac67-ac3d08b9f768 35 fields · synced May 30, 2026