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Skytron Ascend Ip

FDA UDI

Class I (US FDA UDI)

by JAM-Labs Corp.

Identity

Trade Name
SKYTRON ASCEND IP FDA UDI
Generic Name
Medical device integration rack FDA UDI
Device Name
Video Integration Control System FDA UDI
Model / Reference
1.0.0 FDA UDI
Description
Video Integration Control System FDA UDI

Identifiers

Catalog Number
SVIS-ASCENDIP FDA UDI
Primary DI / UDI-DI
00860008848918 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Medical device integration rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device integration rack

Skytron Ascend Ip by JAM-Labs Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device integration rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
JAM-Labs Corp.

Sources (1)

  • FDA UDI 46305b86-5d42-4c54-953f-798098ff9fae 35 fields · synced May 30, 2026