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Neonail

FDA UDI

Class II (US FDA UDI)

by Neoortho Produtos Ortopédicos S/A.

Identity

Trade Name
NEONAIL FDA UDI
Generic Name
Femoral neck fixation sliding bone screw FDA UDI
Device Name
Trochanteric Sliding Starhead Screw D10.5x110 mm FDA UDI
Model / Reference
931.208 FDA UDI
Description
Trochanteric Sliding Starhead Screw D10.5x110 mm FDA UDI

Identifiers

Primary DI / UDI-DI
07899893233335 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Femoral neck fixation sliding bone screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Femoral neck fixation sliding bone screw

Neonail by Neoortho Produtos Ortopédicos S/A. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral neck fixation sliding bone screw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neoortho Produtos Ortopédicos S/A.

Sources (1)

  • FDA UDI cd6ab04b-a62b-4a41-85db-fc9baf65522d 34 fields · synced May 30, 2026