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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Neurosurgical procedure kit, non-medicated, single-use FDA UDI
Device Name
UMMC NEURO MINOR PK, 178633 FDA UDI
Model / Reference
SNE32MNM17 FDA UDI
Description
UMMC NEURO MINOR PK, 178633 FDA UDI

Identifiers

Catalog Number
SNE32MNM17 FDA UDI
Primary DI / UDI-DI
10195594437145 FDA UDI
FDA Product Code
OJG FDA UDI
GMDN Term
Neurosurgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neurosurgical procedure kit, non-medicated, single-use

Cardinal Health Cardinal Health Neuro Surgical Procedure Kit, a comprehensive neurosurgical instrument collection designed for single-use implantable procedures. This sterile kit contains various materials and dressings necessary for safe and effective neurosurgical procedures.

Similar devices

Also classified as Neurosurgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI e45c82cf-be3c-43b1-9cd5-715b2c56be2a 34 fields · synced Jul 21, 2026