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Binder Lift

FDA UDI

Class I (US FDA UDI)

by We Stitch Stuff, LLC

Identity

Trade Name
Binder Lift FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Device Name
Leg Strap Extensions – Sold as a pair FDA UDI
Model / Reference
LSX-BL FDA UDI
Description
Leg Strap Extensions – Sold as a pair FDA UDI

Identifiers

Catalog Number
LSX-BL FDA UDI
Primary DI / UDI-DI
00860011006824 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Manual patient lifting belt/harness FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

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: Manual patient lifting belt/harness

Binder Lift by We Stitch Stuff, LLC — 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

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Manufacturer

Sources (1)

  • FDA UDI 55396ddd-f6eb-4f58-a052-546cb689261d 35 fields · synced Jun 7, 2026