Es2 Spinal System

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: ES2 SPINAL SYSTEM FDA UDI
Generic Name: Bone awl, reusable FDA UDI
Device Name: CANNULATED MODULAR TAP FDA UDI
Model / Reference: 48280185 FDA UDI
Description: CANNULATED MODULAR TAP FDA UDI

Identifiers

Catalog Number: 48280185 FDA UDI
Primary DI / UDI-DI: 07613327003413 FDA UDI
FDA Product Code: ETN FDA UDI
LXH FDA UDI
GMDN Term: Bone awl, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1820 FDA UDI
888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

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: Bone awl, reusable

Es2 Spinal System by Stryker Corp. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 33b11b1d-68fe-409b-8f40-56d6d5ed92a3 35 fields · synced May 30, 2026