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NOVO Health Services, LLC

FDA UDI

Class II (US FDA UDI)

by SRI Healthcare, LLC

Identity

Trade Name
NOVO Health Services, LLC FDA UDI
Generic Name
General surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Set Up Pack, Laparoscopic FDA UDI
Model / Reference
120750 FDA UDI
Description
Set Up Pack, Laparoscopic FDA UDI

Identifiers

Catalog Number
120750D FDA UDI
Primary DI / UDI-DI
00810019802034 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General surgical procedure kit, non-medicated, reusable

NOVO Health Services, LLC by SRI Healthcare, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SRI Healthcare, LLC

Sources (1)

  • FDA UDI cef84971-6f62-45a9-893e-1a5650b862f7 35 fields · synced Jun 8, 2026