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Modified Cooley Rib Spreader

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Modified Cooley Rib Spreader FDA UDI
Generic Name
Rib spreader, reusable FDA UDI
Device Name
Modified Cooley Rib Spreader Child Size Aluminum FDA UDI
Model / Reference
2500-079B FDA UDI
Description
Modified Cooley Rib Spreader Child Size Aluminum FDA UDI

Identifiers

Catalog Number
2500-079B FDA UDI
Primary DI / UDI-DI
00192896120570 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Rib spreader, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 5.5 Inch FDA UDI

Category: Rib spreader, reusable

Modified Cooley Rib Spreader by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rib spreader, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9b12b5fa-7c7c-4135-9439-30dd41a78101 36 fields · synced May 30, 2026