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Probe With Eye

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Probe With Eye FDA UDI
Generic Name
Gastro-urological director FDA UDI
Device Name
Probe With Eye Stainless Steel FDA UDI
Model / Reference
197-666 FDA UDI
Description
Probe With Eye Stainless Steel FDA UDI

Identifiers

Primary DI / UDI-DI
00192896110076 FDA UDI
FDA Product Code
FGM FDA UDI
GMDN Term
Gastro-urological director 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 — 9 Inch FDA UDI

Category: Gastro-urological director

Probe With Eye by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological director.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b351111-eb50-45d7-9d8c-2b4507087814 35 fields · synced Jun 1, 2026