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Balfour Center Blade

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BALFOUR CENTER BLADE FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
BALFOUR CENTER BLADE ADOLESCENT SIZE FDA UDI
Model / Reference
9-5233 FDA UDI
Description
BALFOUR CENTER BLADE ADOLESCENT SIZE FDA UDI

Identifiers

Catalog Number
9-5233 FDA UDI
Primary DI / UDI-DI
00192896072084 FDA UDI
FDA Product Code
FFO FDA UDI
GMDN Term
Self-retaining surgical retractor, 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 — 2 Inch FDA UDI

Category: Self-retaining surgical retractor, reusable

Balfour Center Blade by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cf1cd80c-cd2b-40ba-8b48-43baaf047c07 36 fields · synced Jun 1, 2026