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Turner Warwick Urological Retractor Blade

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
TURNER WARWICK UROLOGICAL RETRACTOR BLADE FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
TURNER WARWICK UROLOGICAL RETRACTOR BLADE FDA UDI
Model / Reference
516-804BB FDA UDI
Description
TURNER WARWICK UROLOGICAL RETRACTOR BLADE FDA UDI

Identifiers

Catalog Number
516-804BB FDA UDI
Primary DI / UDI-DI
00192896080805 FDA UDI
FDA Product Code
FFO FDA UDI
GMDN Term
Surgical retractor/retraction system blade, 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 — 5.375 Inch FDA UDI
Width — 1.125 Inch FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Turner Warwick Urological Retractor Blade by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa4cace5-8340-4e63-854d-a8c9ab3a843e 36 fields · synced May 31, 2026