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NvisionVLE Imaging Probe 17mm Clinical

FDA UDI

Class II (US FDA UDI)

by Ninepoint Medical, Inc.

Identity

Trade Name
NvisionVLE Imaging Probe 17mm Clinical FDA UDI
Generic Name
Endoscopic optical coherence tomography system probe FDA UDI
Model / Reference
95101-17C FDA UDI

Identifiers

Catalog Number
95101-17C FDA UDI
Primary DI / UDI-DI
00859591006157 FDA UDI
510(k) Number
K143678 FDA UDI
FDA Product Code
NQQ FDA UDI
GMDN Term
Endoscopic optical coherence tomography system probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 17 Millimeter FDA UDI

Category: Endoscopic optical coherence tomography system probe

NvisionVLE Imaging Probe 17mm Clinical by Ninepoint Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic optical coherence tomography system probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32e222cb-d034-4f1c-93b2-3f110a34805f 37 fields · synced May 30, 2026