Guide Pin - Bevel

FDA UDI

Class I (US FDA UDI)

by Surgentec Llc

Identity

Trade Name: Guide Pin - Bevel FDA UDI
Generic Name: Orthopaedic bone pin, non-bioabsorbable FDA UDI
Model / Reference: SR99-5006 FDA UDI

Identifiers

Primary DI / UDI-DI: 00810131880910 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Orthopaedic bone pin, non-bioabsorbable 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone pin, non-bioabsorbable

Guide Pin - Bevel by Surgentec Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Surgentec Llc

Sources (1)

FDA UDI 8551e2ac-102f-4bfe-b597-4ad3ca62c5c6 32 fields · synced May 31, 2026