← Back to catalogue

Cooley Bulldog Clamp

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
COOLEY BULLDOG CLAMP FDA UDI
Generic Name
Surgical bulldog clamp, reusable FDA UDI
Device Name
COOLEY BULLDOG CLAMP CROSS ACTION CURVED FDA UDI
Model / Reference
2100-427 FDA UDI
Description
COOLEY BULLDOG CLAMP CROSS ACTION CURVED FDA UDI

Identifiers

Primary DI / UDI-DI
00192896002227 FDA UDI
510(k) Number
K092544 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical bulldog 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 3.375 Inch FDA UDI

Category: Surgical bulldog clamp, reusable

Cooley Bulldog Clamp by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4c3f9f2d-f75d-4c3d-85b0-39869dbbf5f9 36 fields · synced May 31, 2026