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Vasto

FDA UDI

Class I (US FDA UDI)

by US Endoscopy

Identity

Trade Name
Vasto FDA UDI
Generic Name
Endoscopic bite block, basic, single-use FDA UDI
Device Name
The Vasto Bite Block is used to protect the endoscope insertion tube from being bitten by the patient. FDA UDI
Model / Reference
00712810 FDA UDI
Description
The Vasto Bite Block is used to protect the endoscope insertion tube from being bitten by the patient. FDA UDI

Identifiers

Catalog Number
00712810 FDA UDI
Primary DI / UDI-DI
00724995184216 FDA UDI
FDA Product Code
MNK FDA UDI
GMDN Term
Endoscopic bite block, basic, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic bite block, basic, single-use

Vasto by US Endoscopy — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic bite block, basic, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endoscopy

Sources (1)

  • FDA UDI fa828d6f-a6e0-4af5-8abe-33a6984b01d4 36 fields · synced Jun 8, 2026