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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Overbed table FDA UDI
Device Name
Non-Tilt Overbed Table H-BASE ADJUSTABLE HEIGHT | WALNUT |CHROME Table Height 29.13 in - 42.25 in (73.99 cm - 107.32 cm) FDA UDI
Model / Reference
16-11610 FDA UDI
Description
Non-Tilt Overbed Table H-BASE ADJUSTABLE HEIGHT | WALNUT |CHROME Table Height 29.13 in - 42.25 in (73.99 cm - 107.32 cm) FDA UDI

Identifiers

Primary DI / UDI-DI
00612479262393 FDA UDI
FDA Product Code
INW FDA UDI
GMDN Term
Overbed table FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Overbed table

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

Similar devices

Also classified as Overbed table.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI 12d398dd-f945-483d-89f4-18482a494d0d 33 fields · synced Jun 8, 2026