ASTRA Spine System

FDA UDI

Class II (US FDA UDI)

by Spinecraft Llc

Identity

Trade Name: ASTRA Spine System FDA UDI
Generic Name: Implantable bone washer FDA UDI
Device Name: ASTRA Washer, Closed FDA UDI
Model / Reference: A5W-C FDA UDI
Description: ASTRA Washer, Closed FDA UDI

Identifiers

Catalog Number: A5W-C FDA UDI
Primary DI / UDI-DI: 00193082075506 FDA UDI
FDA Product Code: MNH FDA UDI
KWP FDA UDI
KWQ FDA UDI
NKB FDA UDI
MNI FDA UDI
GMDN Term: Implantable bone washer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3050 FDA UDI
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

Category: Implantable bone washer

ASTRA Spine System by Spinecraft Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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LEOS Cannulated Screw System — Tyber Medical · 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: Spinecraft Llc

Sources (1)

FDA UDI c65c1aa2-aef3-4539-8e93-f9393f1ea975 35 fields · synced Jun 8, 2026