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Valeo Spacer System

FDA UDI

Class II (US FDA UDI)

by Amedica Corp.

Identity

Trade Name
Valeo Spacer System FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Case 1, Tray 1 - Valeo C FDA UDI
Model / Reference
D FDA UDI
Description
Case 1, Tray 1 - Valeo C FDA UDI

Identifiers

Catalog Number
91.002.0003 FDA UDI
Primary DI / UDI-DI
M555910020003 FDA UDI
FDA Product Code
ODP FDA UDI
MAX FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Over-the-Counter

Yes

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

Valeo Spacer System by Amedica Corp. — 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

Manufacturer
Amedica Corp.

Sources (1)

  • FDA UDI 345592bd-4ed0-48ae-85a6-d7ac5c54916c 36 fields · synced Jun 6, 2026