nvt

FDA UDI

Class I (US FDA UDI)

by Nvision Biomedical Technologies, Inc

Identity

Trade Name: nvt FDA UDI
Generic Name: Surgical tamp, reusable FDA UDI
Device Name: Instrument, Trial, Transforaminal Lumbar Interbody Fusion System (TLIF) FDA UDI
Model / Reference: TL-1135T-710 FDA UDI
Description: Instrument, Trial, Transforaminal Lumbar Interbody Fusion System (TLIF) FDA UDI

Identifiers

Primary DI / UDI-DI: 00814008022151 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: Surgical tamp, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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Implantable

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Contains Latex

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Prescription Use

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Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

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Premarket Exempt

Yes

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Angle — 7 degree FDA UDI
Length — 11 Millimeter FDA UDI
Width — 35 Millimeter FDA UDI
Height — 10 Millimeter FDA UDI

Category: Surgical tamp, reusable

nvt by Nvision Biomedical Technologies, Inc — 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: Nvision Biomedical Technologies, Inc

Sources (1)

FDA UDI 76a2a06e-429d-4773-b50e-a13166973fc1 35 fields · synced Jun 8, 2026