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Vaccine Administration Kit, Facility

FDA UDI

Class II (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
Vaccine Administration Kit, Facility FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
The Vaccine Administration Kit, Facility, contains the necessary items to prepare up to 100 patients for inoculation. FDA UDI
Model / Reference
04656 FDA UDI
Description
The Vaccine Administration Kit, Facility, contains the necessary items to prepare up to 100 patients for inoculation. FDA UDI

Identifiers

Catalog Number
04656 FDA UDI
Primary DI / UDI-DI
00850018892919 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

Vaccine Administration Kit, Facility by Altitude Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General 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
Altitude Technologies Inc.

Sources (1)

  • FDA UDI 36071ab2-ff77-4da8-8972-b5de2d3d9ba0 35 fields · synced May 30, 2026