← Back to catalogue

ManaMed

FDA UDI

Class I (US FDA UDI)

by Manamed Llc

Identity

Trade Name
ManaMed FDA UDI
Generic Name
Shoulder immobilizer/orthosis, reusable FDA UDI
Device Name
The EZ Sling Universal shoulder immobilizer includes a waist strap. For use with the treatment of: • Surgical repair of rotator cuff • Anterior dislocation of the G-H joint • Anterior glenohumeral capsular reconstruction • S/P glenohumeral acromioplasty Simple and comfortable Universal Sizing FDA UDI
Model / Reference
ManaEZ Sling Universal FDA UDI
Description
The EZ Sling Universal shoulder immobilizer includes a waist strap. For use with the treatment of: • Surgical repair of rotator cuff • Anterior dislocation of the G-H joint • Anterior glenohumeral capsular reconstruction • S/P glenohumeral acromioplasty Simple and comfortable Universal Sizing FDA UDI

Identifiers

Catalog Number
EZSLUNI FDA UDI
Primary DI / UDI-DI
00810113680736 FDA UDI
FDA Product Code
ILI FDA UDI
GMDN Term
Shoulder immobilizer/orthosis, reusable 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

No

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

Yes

FDA UDI

Category: Shoulder immobilizer/orthosis, reusable

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

Similar devices

Also classified as Shoulder immobilizer/orthosis, reusable.

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
Manamed Llc

Sources (1)

  • FDA UDI 1c4cbe8f-77d6-4eff-8d36-ffa28612730e 35 fields · synced May 31, 2026