← Back to catalogue

Frame-Harness Strap Set

FDA UDI

Class II (US FDA UDI)

by Xact Robotics Ltd

Identity

Trade Name
Frame-Harness Strap Set FDA UDI
Generic Name
Medical/surgical interventional tube/cable securement strap FDA UDI
Device Name
Frame-Harness Strap Set FDA UDI
Model / Reference
A FDA UDI
Description
Frame-Harness Strap Set FDA UDI

Identifiers

Catalog Number
XR-FRM-HRN FDA UDI
Primary DI / UDI-DI
07290017702278 FDA UDI
510(k) Number
K191332 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Medical/surgical interventional tube/cable securement strap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical/surgical interventional tube/cable securement strap

Frame-Harness Strap Set by Xact Robotics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical/surgical interventional tube/cable securement strap.

Cleared under the same submission

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

Manufacturer
Xact Robotics Ltd

Sources (1)

  • FDA UDI 709649c8-c80f-48eb-8eab-b9aa25b1bfbc 36 fields · synced Jun 8, 2026