Ambassador

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name: Ambassador FDA UDI
Generic Name: Spinal fixation plate, non-bioabsorbable FDA UDI
Model / Reference: 05-100-02-0036 FDA UDI

Identifiers

Catalog Number: 05-100-02-0036 FDA UDI
Primary DI / UDI-DI: 10885862262998 FDA UDI
FDA Product Code: KWQ FDA UDI
GMDN Term: Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3060 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 36 Millimeter FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

Ambassador by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Spinal fixation plate, non-bioabsorbable.

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PROVIDENCE — GLOBUS MEDICAL, INC. · Class II
ACP — Nuvasive, Inc. · Class II
uNion Cervical Plate System — ULRICH MEDICAL USA, INC. · Class II

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: Choicespine, LP

Sources (1)

FDA UDI 6bf95267-7a38-4faf-a59c-8b305c4a1a62 34 fields · synced May 31, 2026