← Back to catalogue

Binder Lift

FDA UDI

Class I (US FDA UDI)

by We Stitch Stuff, LLC

Identity

Trade Name
Binder Lift FDA UDI
Generic Name
Patient transfer/turning sheet, reusable FDA UDI
Device Name
Binder Transfer Anchors (set of 8) for Stryker Pro XT and Pro 2 models FDA UDI
Model / Reference
BT-SA3-BL FDA UDI
Description
Binder Transfer Anchors (set of 8) for Stryker Pro XT and Pro 2 models FDA UDI

Identifiers

Catalog Number
BT-SA3-BL FDA UDI
Primary DI / UDI-DI
00860012552160 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer/turning sheet, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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: Patient transfer/turning sheet, reusable

Binder Lift by We Stitch Stuff, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer/turning sheet, 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

Sources (1)

  • FDA UDI 6e9e1b5e-76b5-4fd1-8d45-e47fdbaba9c2 35 fields · synced May 30, 2026