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Universal Arm Sling

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
UNIVERSAL ARM SLING FDA UDI
Generic Name
Elevation arm sling FDA UDI
Model / Reference
08140015 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570166756 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Elevation arm sling

Universal Arm Sling by Bird & Cronin, Llc — 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

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Manufacturer

Manufacturer
Bird & Cronin, Llc

Sources (1)

  • FDA UDI e9845a1d-0780-414f-9e16-9dc3fa976221 32 fields · synced Jun 6, 2026