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Versa-Sling Kit Universal

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
VERSA-SLING KIT UNIVERSAL FDA UDI
Generic Name
Elevation arm sling FDA UDI
Model / Reference
90008250 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570178858 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

Versa-Sling Kit Universal 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 ce23a5dc-2c0d-472a-a367-7235bd95c681 32 fields · synced May 31, 2026