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Orthopaedic Manual Surgical Instruments

FDA UDI

Class I (US FDA UDI)

by Citieffe

Identity

Trade Name
ORTHOPAEDIC MANUAL SURGICAL INSTRUMENTS FDA UDI
Generic Name
Medical ruler, single-use FDA UDI
Model / Reference
Screws ruler kit Guide wire, trocar tip ø3x420mm FDA UDI

Identifiers

Catalog Number
VT-96440 FDA UDI
Primary DI / UDI-DI
08059386747681 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Medical ruler, single-use 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

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

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: Medical ruler, single-use

Orthopaedic Manual Surgical Instruments by Citieffe — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical ruler, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Citieffe

Sources (1)

  • FDA UDI 7b10b657-28f6-449a-ab94-e87773c45113 35 fields · synced Jun 6, 2026