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PRECICE® Trauma Intramedullary Nail System Instrument

FDA UDI

Class II (US FDA UDI)

by NuVasive Specialized Orthopedics, Inc.

Identity

Trade Name
PRECICE® Trauma Intramedullary Nail System Instrument FDA UDI
Generic Name
Humerus intramedullary nail FDA UDI
Device Name
Orthopedic surgical instrument (proximal guide) - for use with the trauma intramedullary rod, humerus FDA UDI
Model / Reference
HPG1-000 FDA UDI
Description
Orthopedic surgical instrument (proximal guide) - for use with the trauma intramedullary rod, humerus FDA UDI

Identifiers

Catalog Number
HPG1-000 FDA UDI
Primary DI / UDI-DI
00812258028183 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Humerus intramedullary nail 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Humerus intramedullary nail

PRECICE® Trauma Intramedullary Nail System Instrument by NuVasive Specialized Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Humerus intramedullary nail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
NuVasive Specialized Orthopedics, Inc.

Sources (1)

  • FDA UDI 395f1295-7aec-41d1-87bf-e32a67b2966f 36 fields · synced Jun 1, 2026