← Back to catalogue

restor3d Lumbar Instrument

FDA UDI

Class I (US FDA UDI)

by Restor3D

Identity

Trade Name
restor3d Lumbar Instrument FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
ALIF Instruments - Lid FDA UDI
Model / Reference
5113-A0012 FDA UDI
Description
ALIF Instruments - Lid FDA UDI

Identifiers

Primary DI / UDI-DI
00840097508849 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, 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

No

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: Instrument tray, reusable

restor3d Lumbar Instrument by Restor3D — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Restor3D

Sources (1)

  • FDA UDI 80623a03-0aa3-4c14-a784-6f17b76bf0c9 33 fields · synced May 30, 2026