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Zimmer® Cannulated Screw System

FDA UDI

Class I (US FDA UDI)

by Pioneer Surgical Technology, Inc.

Identity

Trade Name
Zimmer® Cannulated Screw System FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI
Device Name
STYLET, 1.25mm FDA UDI
Model / Reference
00-1147-070-00 FDA UDI
Description
STYLET, 1.25mm FDA UDI

Identifiers

Catalog Number
00-1147-070-00 FDA UDI
Primary DI / UDI-DI
00846468074333 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical instrument/endoscope cleaning utensil, reusable 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

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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument/endoscope cleaning utensil, reusable

Zimmer® Cannulated Screw System by Pioneer Surgical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pioneer Surgical Technology, Inc.

Sources (1)

  • FDA UDI f024e66c-93ae-46fe-8f8c-998954d80d42 35 fields · synced Jun 1, 2026