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DeRoyal

FDA UDI

Class I (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Obstetrical/gynaecological surgical procedure kit, medicated FDA UDI
Device Name
C-SECTION TRAY PGYBK FDA UDI
Model / Reference
89-3275 FDA UDI
Description
C-SECTION TRAY PGYBK FDA UDI

Identifiers

Catalog Number
89-3275 FDA UDI
Primary DI / UDI-DI
00749756337106 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Obstetrical/gynaecological surgical procedure kit, medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Category: Obstetrical/gynaecological surgical procedure kit, medicated

DeRoyal by Deroyal Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Obstetrical/gynaecological surgical procedure kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Deroyal Industries, Inc.

Sources (1)

  • FDA UDI 2769e30f-1436-4ff2-bcbc-d4d94678a71c 35 fields · synced Jun 8, 2026