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All-Poly Tibial Broach Tower Assembly

FDA UDI

Class I (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name
All-Poly Tibial Broach Tower Assembly FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Device Name
All-Poly Tibial Broach Tower Assembly, Sizes 5-6 FDA UDI
Model / Reference
2215.05.000 FDA UDI
Description
All-Poly Tibial Broach Tower Assembly, Sizes 5-6 FDA UDI

Identifiers

Primary DI / UDI-DI
00819251023153 FDA UDI
FDA Product Code
HTQ FDA UDI
GMDN Term
Orthopaedic broach 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 broach

All-Poly Tibial Broach Tower Assembly by Total Joint Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic broach.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c10152c-c06a-40cc-92ad-5e99e4b65c9b 36 fields · synced May 30, 2026