Dingo Clamp

FDA UDI

Class II (US FDA UDI)

by Vitalcor, Inc

Identity

Trade Name: Dingo Clamp FDA UDI
Generic Name: Vascular clamp, reusable FDA UDI
Device Name: Titanium Micro Vascular Clamp - 7.9mm FDA UDI
Model / Reference: VA079-06 FDA UDI
Description: Titanium Micro Vascular Clamp - 7.9mm FDA UDI

Identifiers

Catalog Number: VA079-06 FDA UDI
Primary DI / UDI-DI: 00851321006499 FDA UDI
510(k) Number: K070661 FDA UDI
FDA Product Code: DXC FDA UDI
GMDN Term: Vascular clamp, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4450 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Vascular clamp, reusable

Dingo Clamp by Vitalcor, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Vascular clamp, reusable.

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Novo Surgical — NOVO SURGICAL, INC. · Class II
SCANLAN® — SCANLAN INTERNATIONAL INC · Class II

Cleared under the same submission

K070661 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Vitalcor, Inc

Sources (1)

FDA UDI 4eade6d8-4601-4079-9772-3fb0df354cfd 36 fields · synced Jun 8, 2026