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Remedy Broach

FDA UDI

Class II (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Remedy Broach FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Model / Reference
111-19-6210 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215040017 FDA UDI
510(k) Number
K133370 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
JDI FDA UDI
KWY FDA UDI
LXH FDA UDI
GMDN Term
Orthopaedic broach FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
888.3350 FDA UDI
888.3390 FDA UDI
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

Yes

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

Remedy Broach by Signature Orthopaedics Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic broach.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a1148eb3-9049-44b2-8142-1d2af9964413 33 fields · synced May 30, 2026