← Back to catalogue

Merits

FDA UDI

Class I (US FDA UDI)

by Merits Health Products., Inc.

Identity

Trade Name
MERITS FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Model / Reference
H101B-CPMU FDA UDI

Identifiers

Primary DI / UDI-DI
04714379291957 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Manual patient lifting belt/harness FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual patient lifting belt/harness

Merits by Merits Health Products., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual patient lifting belt/harness.

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

Sources (1)

  • FDA UDI 3593bcd7-28ce-48e5-9c2d-d79bb17e06ee 32 fields · synced Jun 8, 2026