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Sr Pip

FDA UDI

Class Unclassified (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
SR PIP FDA UDI
Generic Name
Orthopaedic broach FDA UDI
Device Name
SIZE 3: PIP PROXIMAL BROACH ASSEMBLY (ORANGE) FDA UDI
Model / Reference
17-1327 FDA UDI
Description
SIZE 3: PIP PROXIMAL BROACH ASSEMBLY (ORANGE) FDA UDI

Identifiers

Primary DI / UDI-DI
00886385019864 FDA UDI
FDA Product Code
MPK FDA UDI
GMDN Term
Orthopaedic broach FDA UDI

Classification

Device Class
Unclassified 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

Sr Pip by Stryker Corp. — Class Unclassified — 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

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 05394005-e9eb-47ff-9732-d248a48c993f 34 fields · synced May 31, 2026