← Back to catalogue

Vorse Tube Occluding Clamp

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
VORSE TUBE OCCLUDING CLAMP FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
Device Name
TUBE OCCLUDING CLAMP SERRATED WITH U-SHAPED GUARD FDA UDI
Model / Reference
117-568 FDA UDI
Description
TUBE OCCLUDING CLAMP SERRATED WITH U-SHAPED GUARD FDA UDI

Identifiers

Primary DI / UDI-DI
B0991175680 FDA UDI
FDA Product Code
GDJ FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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 — 8 Inch FDA UDI

Vorse Tube Occluding Clamp by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 9c94f53d-a450-42ee-987a-0a6a3fdb5539 36 fields · synced Jun 1, 2026