← Back to catalogue

Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
General specimen container IVD, no additive/medium FDA UDI
Device Name
GRADUATED PITCHER STERILE 1000 CC FDA UDI
Model / Reference
GR100150ST FDA UDI
Description
GRADUATED PITCHER STERILE 1000 CC FDA UDI

Identifiers

Catalog Number
GR100150ST FDA UDI
Primary DI / UDI-DI
10653160273554 FDA UDI
FDA Product Code
KYW FDA UDI
GMDN Term
General specimen container IVD, no additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen container IVD, no additive/medium

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

Similar devices

Also classified as General specimen container IVD, no additive/medium.

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
Centurion Medical Products

Sources (1)

  • FDA UDI 9dac2cc1-bda1-4bb8-8b5b-d93a63caad85 35 fields · synced Jun 8, 2026