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PyroCarbon PIP Total Joint System

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
PyroCarbon PIP Total Joint System FDA UDI
Generic Name
Bone cutter FDA UDI
Device Name
PIP DISPOSABLE PACK FOR STRYKER FDA UDI
Model / Reference
PIP-DIS-STR FDA UDI
Description
PIP DISPOSABLE PACK FOR STRYKER FDA UDI

Identifiers

Catalog Number
PIP-DIS-STR FDA UDI
Primary DI / UDI-DI
00885556858486 FDA UDI
FDA Product Code
HTZ FDA UDI
HAB FDA UDI
HTT FDA UDI
FZX FDA UDI
GMDN Term
Bone cutter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
878.4820 FDA UDI
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone cutter

PyroCarbon PIP Total Joint System by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 282fd9d4-e3f8-4337-8001-9cf751a7747e 35 fields · synced Jun 8, 2026