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Morrison Medical

FDA UDI

Class I (US FDA UDI)

by Morrison Medical, Ltd

Identity

Trade Name
MORRISON MEDICAL FDA UDI
Generic Name
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
OB KIT WITH FOIL BABY BUNTING FDA UDI
Model / Reference
0969 FDA UDI
Description
OB KIT WITH FOIL BABY BUNTING FDA UDI

Identifiers

Catalog Number
0969 FDA UDI
Primary DI / UDI-DI
00647921096905 FDA UDI
FDA Product Code
OKU FDA UDI
GMDN Term
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use

Morrison Medical by Morrison Medical, Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Morrison Medical, Ltd

Sources (1)

  • FDA UDI ff1b9f22-8437-46fe-9960-2cfabcc8f4ad 35 fields · synced Jun 6, 2026