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Sontec Sternal Rib Spreader Retractor

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SONTEC STERNAL RIB SPREADER RETRACTOR FDA UDI
Generic Name
Rib spreader, reusable FDA UDI
Device Name
SONTEC STERNAL RIB SPREADER RETRACTOR CONCAVE/CONVEX BLADES CHILD SIZE ALUMINUM FDA UDI
Model / Reference
2500-062A FDA UDI
Description
SONTEC STERNAL RIB SPREADER RETRACTOR CONCAVE/CONVEX BLADES CHILD SIZE ALUMINUM FDA UDI

Identifiers

Catalog Number
2500-062A FDA UDI
Primary DI / UDI-DI
00192896086678 FDA UDI
FDA Product Code
FFO FDA UDI
GMDN Term
Rib spreader, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Dimensions & Sizes

Size
Length — 4 Inch FDA UDI

Category: Rib spreader, reusable

Sontec Sternal Rib Spreader Retractor 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 c52dfbdf-fc18-4632-9cb9-511cb4057296 36 fields · synced May 30, 2026