← Back to catalogue

Redicare

FDA UDI

Class I (US FDA UDI)

by Redicare Llc

Identity

Trade Name
Redicare FDA UDI
Generic Name
Suspension arm sling FDA UDI
Device Name
1 Triangular Bandage 40x40x56 inch with Clips 1/box FDA UDI
Model / Reference
Triangular Bandage FDA UDI
Description
1 Triangular Bandage 40x40x56 inch with Clips 1/box FDA UDI

Identifiers

Primary DI / UDI-DI
B70901130070 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Suspension arm sling FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

Category: Suspension arm sling

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

Similar devices

Also classified as Suspension 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

Manufacturer
Redicare Llc

Sources (1)

  • FDA UDI 8f7b0ffd-b992-4a98-ba69-d5852c252fa3 34 fields · synced Jun 6, 2026