← Back to catalogue

Centurion

FDA UDI

Class II (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
General surgical procedure kit, medicated FDA UDI
Device Name
CIRCUMCISION TRAY FDA UDI
Model / Reference
CIT7050C FDA UDI
Description
CIRCUMCISION TRAY FDA UDI

Identifiers

Catalog Number
CIT7050C FDA UDI
Primary DI / UDI-DI
10653160361978 FDA UDI
510(k) Number
K213481 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
General surgical procedure kit, medicated 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

No

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

No

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 surgical procedure kit, medicated

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

Similar devices

Also classified as General surgical procedure kit, medicated.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 92055ba3-1d30-4ef3-85f5-5ab803cc241c 36 fields · synced Jun 8, 2026