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McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Basic power supply, reusable FDA UDI
Device Name
Premium GS 777 Integrated Wall System PANOPTIC PLUS | SURETEMP® PLUS FDA UDI
Model / Reference
156-4PM3 FDA UDI
Description
Premium GS 777 Integrated Wall System PANOPTIC PLUS | SURETEMP® PLUS FDA UDI

Identifiers

Primary DI / UDI-DI
10612479260419 FDA UDI
FDA Product Code
HLI FDA UDI
GMDN Term
Basic power supply, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1570 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic power supply, reusable

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

Similar devices

Also classified as Basic power supply, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a850a0cd-3e65-487b-9439-53c3a208677d 33 fields · synced May 31, 2026