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ManaMed

FDA UDI

Class I (US FDA UDI)

by Manamed Llc

Identity

Trade Name
ManaMed FDA UDI
Generic Name
Pelvic fracture binder, reusable FDA UDI
Device Name
Wrap the belt around your belly while making sure the pad is centered and placed under your abdomen for comfort and support. Hand wash in cold water with mild detergent Air dry FDA UDI
Model / Reference
Belly Band FDA UDI
Description
Wrap the belt around your belly while making sure the pad is centered and placed under your abdomen for comfort and support. Hand wash in cold water with mild detergent Air dry FDA UDI

Identifiers

Catalog Number
BB001 FDA UDI
Primary DI / UDI-DI
00810113680163 FDA UDI
FDA Product Code
ISR FDA UDI
GMDN Term
Pelvic fracture binder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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: Pelvic fracture binder, reusable

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

Similar devices

Also classified as Pelvic fracture binder, 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 896d4688-5d39-479e-b110-32264f8a8d19 34 fields · synced Jun 8, 2026