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VerteFIT

FDA UDI

Class I (US FDA UDI)

by Ldr Spine USA

Identity

Trade Name
VerteFIT FDA UDI
Generic Name
Orthopaedic bone calliper FDA UDI
Model / Reference
VF9110R FDA UDI

Identifiers

Catalog Number
VF9110R FDA UDI
Primary DI / UDI-DI
03662663033213 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic bone calliper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 100 Millimeter FDA UDI

Category: Orthopaedic bone calliper

VerteFIT by Ldr Spine USA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone calliper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ldr Spine USA

Sources (1)

  • FDA UDI 02cff166-90f4-4506-bbd5-1a6378bbc610 35 fields · synced May 30, 2026