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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
Basic power supply, reusable FDA UDI
Device Name
GS 777 Integrated Wall System COAXIAL | SURETEMP® PLUS FDA UDI
Model / Reference
156-4L FDA UDI
Description
GS 777 Integrated Wall System COAXIAL | SURETEMP® PLUS FDA UDI

Identifiers

Primary DI / UDI-DI
10612479259437 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Basic power supply, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1860 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

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

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 I — 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 1fff2481-a08b-4bb9-97a6-537909addd21 33 fields · synced Jun 8, 2026