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Centurion

FDA UDI

Class II (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Lumbar puncture kit FDA UDI
Device Name
ADULT LUMBAR PUNCTURE TRAY FDA UDI
Model / Reference
MNS8745A FDA UDI
Description
ADULT LUMBAR PUNCTURE TRAY FDA UDI

Identifiers

Catalog Number
MNS8745A FDA UDI
Primary DI / UDI-DI
10653160343325 FDA UDI
FDA Product Code
PWY FDA UDI
GMDN Term
Lumbar puncture kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

Yes

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

No

FDA UDI

Category: Lumbar puncture kit

Centurion by Centurion Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lumbar puncture kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centurion Medical Products

Sources (1)

  • FDA UDI cc8c89db-90f9-4969-a689-102c3ec8cfc3 35 fields · synced May 31, 2026