2.2mm Mini-Bolt VUE

FDA UDI

Class I (US FDA UDI)

by Monteris Medical Corp

Identity

Trade Name: 2.2mm Mini-Bolt VUE FDA UDI
Generic Name: Neurological stereotactic surgery system FDA UDI
Device Name: 2.2mm Mini-Bolt VUE Sterile Packaged FDA UDI
Model / Reference: 21122 FDA UDI
Description: 2.2mm Mini-Bolt VUE Sterile Packaged FDA UDI

Identifiers

Catalog Number: CMB022-V FDA UDI
Primary DI / UDI-DI: 00816589022322 FDA UDI
FDA Product Code: HAO FDA UDI
GMDN Term: Neurological stereotactic surgery system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4535 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 2.2 Millimeter FDA UDI

Category: Neurological stereotactic surgery system

2.2mm Mini-Bolt VUE by Monteris Medical Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Monteris Medical Corp

Sources (1)

FDA UDI e99903df-0333-4623-a3ca-4651cbb27a5d 36 fields · synced Jun 6, 2026