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Debakey Retractor

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Debakey Retractor FDA UDI
Generic Name
Rib spreader, reusable FDA UDI
Device Name
Debakey Retractor Child Size 3 Pairs of Blades 6.875 Inch Spread FDA UDI
Model / Reference
2500-550 FDA UDI
Description
Debakey Retractor Child Size 3 Pairs of Blades 6.875 Inch Spread FDA UDI

Identifiers

Primary DI / UDI-DI
00192896108387 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

Category: Rib spreader, reusable

Debakey 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 2b2acdea-0773-4e55-95c3-0b44b6a570cd 34 fields · synced May 30, 2026