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Luna Supine Pad System

FDA UDI

Class I (US FDA UDI)

by Infinitus Medical Technologies Llc

Identity

Trade Name
LUNA SUPINE PAD SYSTEM FDA UDI
Generic Name
Operating table patient positioning set, single-use FDA UDI
Model / Reference
SP-3500 FDA UDI

Identifiers

Primary DI / UDI-DI
00860006375959 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Operating table patient positioning set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Operating table patient positioning set, single-use

Luna Supine Pad System by Infinitus Medical Technologies Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating table patient positioning set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f3a59321-4d3f-4e20-8c74-0974ccdc78bb 32 fields · synced Jun 8, 2026