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V.a.t.s Duval Clamp

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
V.A.T.S DUVAL CLAMP FDA UDI
Generic Name
Surgical bulldog clamp, reusable FDA UDI
Device Name
V.A.T.S. DUVAL CLAMP WITHOUT RATCHET DEBAKEY JAW CURVED FDA UDI
Model / Reference
2100-825A FDA UDI
Description
V.A.T.S. DUVAL CLAMP WITHOUT RATCHET DEBAKEY JAW CURVED FDA UDI

Identifiers

Primary DI / UDI-DI
B0992100825A0 FDA UDI
510(k) Number
K152400 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical bulldog clamp, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 13 Millimeter FDA UDI

V.a.t.s Duval Clamp by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 8a8c1c3b-e549-4a4f-8a30-08431dd33460 37 fields · synced Jun 8, 2026