← Back to catalogue

MOTOBAND Instruments

FDA UDI

Class I (US FDA UDI)

by Crossroads Extremity Systems Llc

Identity

Trade Name
MOTOBAND Instruments FDA UDI
Generic Name
Orthopaedic surgical distractor, internal FDA UDI
Device Name
HINTERMANN DISTRACTOR, GSOURCE FDA UDI
Model / Reference
HINTERMANN DISTRACTOR, GSOURCE FDA UDI
Description
HINTERMANN DISTRACTOR, GSOURCE FDA UDI

Identifiers

Catalog Number
280268PKG FDA UDI
Primary DI / UDI-DI
00810112598070 FDA UDI
FDA Product Code
HWB FDA UDI
GMDN Term
Orthopaedic surgical distractor, internal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical distractor, internal

MOTOBAND Instruments by Crossroads Extremity Systems Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical distractor, internal.

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
Crossroads Extremity Systems Llc

Sources (1)

  • FDA UDI 7872e685-82ab-4400-82ee-91f6a172b6a3 34 fields · synced May 29, 2026