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Sling & Swathe Immobilizer Lg

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
SLING & SWATHE IMMOBILIZER LG FDA UDI
Generic Name
Shoulder immobilizer/orthosis, single-use FDA UDI
Model / Reference
08140164 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570001507 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Shoulder immobilizer/orthosis, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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: Shoulder immobilizer/orthosis, single-use

Sling & Swathe Immobilizer Lg by Bird & Cronin, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoulder immobilizer/orthosis, single-use.

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 dc62d04c-22af-4e23-95aa-c8aa055638b3 32 fields · synced May 30, 2026