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ManaMed

FDA UDI

Class I (US FDA UDI)

by Manamed Llc

Identity

Trade Name
ManaMed FDA UDI
Generic Name
Tubular support bandage, non-latex, reusable FDA UDI
Device Name
The ManaEZ Tendon Strap Universal is used to soothe tennis elbow pain. Low profile, neoprene strap, gel pad for compression FDA UDI
Model / Reference
ManaEZ Tendon Strap Universal FDA UDI
Description
The ManaEZ Tendon Strap Universal is used to soothe tennis elbow pain. Low profile, neoprene strap, gel pad for compression FDA UDI

Identifiers

Catalog Number
EZTS01 FDA UDI
Primary DI / UDI-DI
00810113680767 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Tubular support bandage, non-latex, reusable 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

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: Tubular support bandage, non-latex, reusable

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

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Manamed Llc

Sources (1)

  • FDA UDI 2b39e307-d4ff-4d47-a4ae-315cd18de7b9 35 fields · synced May 29, 2026