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Redicare

FDA UDI

Class I (US FDA UDI)

by Redicare Llc

Identity

Trade Name
Redicare FDA UDI
Generic Name
First aid limb splint, mouldable, single-use FDA UDI
Device Name
4.25" x 24" Padded Aluminum Conforming Splint FDA UDI
Model / Reference
Redisplint Conforming Splint FDA UDI
Description
4.25" x 24" Padded Aluminum Conforming Splint FDA UDI

Identifiers

Catalog Number
0305006 FDA UDI
Primary DI / UDI-DI
B70903050060 FDA UDI
FDA Product Code
NOC FDA UDI
GMDN Term
First aid limb splint, mouldable, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3910 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

Yes

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

Dimensions & Sizes

Size
Width — 4.25 Inch FDA UDI
Length — 24 Inch FDA UDI

Category: First aid limb splint, mouldable, single-use

Redicare by Redicare Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid limb splint, mouldable, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Redicare Llc

Sources (1)

  • FDA UDI 25de8351-61cb-412a-b597-aeea87fd1400 35 fields · synced May 31, 2026