← Back to catalogue

Sontec Rectal Blade

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Sontec Rectal Blade FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Sontec Rectal Blade 167 Millimeters X 95 Millimeters FDA UDI
Model / Reference
516-880 FDA UDI
Description
Sontec Rectal Blade 167 Millimeters X 95 Millimeters FDA UDI

Identifiers

Primary DI / UDI-DI
00192896109001 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

Category: Surgical retractor/retraction system blade, reusable

Sontec Rectal 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 638189ff-a5e3-49ce-a47a-05b664317b94 34 fields · synced Jun 6, 2026