← Back to catalogue

Sannio Aeovis

FDA UDI

Class I (US FDA UDI)

by The Sannio Group Inc

Identity

Trade Name
Sannio Aeovis FDA UDI
Generic Name
Elevation arm sling FDA UDI
Device Name
This stainless steel device is customizable to the patient and provides the framework for Sannio Group mesh. Customization allows the device to work with any hospital bed height and incline, and the device can be adjusted to support the arm at different angles. FDA UDI
Model / Reference
1 FDA UDI
Description
This stainless steel device is customizable to the patient and provides the framework for Sannio Group mesh. Customization allows the device to work with any hospital bed height and incline, and the device can be adjusted to support the arm at different angles. FDA UDI

Identifiers

Primary DI / UDI-DI
00860006225018 FDA UDI
FDA Product Code
ILI FDA UDI
GMDN Term
Elevation arm sling FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3640 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

Yes

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

Dimensions & Sizes

Size
Length — 44 Inch FDA UDI
Width — 14 Inch FDA UDI

Category: Elevation arm sling

Sannio Aeovis by The Sannio Group Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Elevation arm sling.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0c4705e7-5cac-4832-a8bc-cd8de13d44b3 34 fields · synced May 30, 2026