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General Instrument

FDA UDI

Class I (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
General Instrument FDA UDI
Generic Name
Bone lever/elevator, reusable FDA UDI
Device Name
Lollipop Cobb, Caudal, 18mm FDA UDI
Model / Reference
CI-10740-400-18 FDA UDI
Description
Lollipop Cobb, Caudal, 18mm FDA UDI

Identifiers

Primary DI / UDI-DI
00840180505847 FDA UDI
FDA Product Code
HTE FDA UDI
GMDN Term
Bone lever/elevator, reusable FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone lever/elevator, reusable

General Instrument by Alphatec Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone lever/elevator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alphatec Spine, Inc.

Sources (1)

  • FDA UDI 29c53f5c-93a2-4fc8-9404-be4ead7fc10e 34 fields · synced Jun 8, 2026