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PS-Post Box Resection Guide

FDA UDI

Class I (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name
PS-Post Box Resection Guide FDA UDI
Generic Name
Orthopaedic reamer guide FDA UDI
Device Name
PS-Post Box Resection Guide, Size 1 FDA UDI
Model / Reference
2172.01.000 FDA UDI
Description
PS-Post Box Resection Guide, Size 1 FDA UDI

Identifiers

Primary DI / UDI-DI
00810094691851 FDA UDI
FDA Product Code
LXH FDA UDI
HTO FDA UDI
GMDN Term
Orthopaedic reamer guide 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

No

FDA UDI

Lot / Batch Number

No

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

Category: Orthopaedic reamer guide

PS-Post Box Resection Guide by Total Joint Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic reamer guide.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd0220f3-9537-4c8b-bc94-856bf5afe9e3 36 fields · synced May 31, 2026