McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name: McKesson FDA UDI
Generic Name: Perineal/coccygeal cushion FDA UDI
Device Name: Compressed lumbar cush 13.5x13x4 FDA UDI
Model / Reference: 146-RTL1493COM FDA UDI
Description: Compressed lumbar cush 13.5x13x4 FDA UDI

Identifiers

Primary DI / UDI-DI: 00612479231429 FDA UDI
FDA Product Code: IQK FDA UDI
GMDN Term: Perineal/coccygeal cushion FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3490 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Perineal/coccygeal cushion

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Ever-Soft Coccyx Gel Foam Cushion, 20"x16"x3" — Dynarex Corp. · Class I
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ROSCOE MEDICAL — COMPASS HEALTH BRANDS CORP. · U
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ContourMD — ContourMD Marketing Group, LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Mckesson Medical-Surgical Inc.

Sources (1)

FDA UDI 1bfb38a7-236c-42a4-a93d-5d8ffac3a1d1 33 fields · synced May 30, 2026