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Screw, Cann., 7.0mmx50mm, 24mm Thread

FDA UDI

Class II (US FDA UDI)

by Pioneer Surgical Technology, Inc.

Identity

Trade Name
Screw, Cann., 7.0mmx50mm, 24mm Thread FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
7.0mmx50mm, 24mm Thread FDA UDI
Model / Reference
431-694-050 FDA UDI
Description
7.0mmx50mm, 24mm Thread FDA UDI

Identifiers

Catalog Number
431-694-050 FDA UDI
Primary DI / UDI-DI
00846468041991 FDA UDI
FDA Product Code
HWC FDA UDI
OUR FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Screw, Cann., 7.0mmx50mm, 24mm Thread by Pioneer Surgical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a60f16a-2be4-4bb4-ba3f-d1fcfb3f76d8 36 fields · synced May 31, 2026