McConnell Orthopedic MFG. CO.

FDA UDI

Class I (US FDA UDI)

by Mcconnell Orthopedic Mfg. Co.

Identity

Trade Name: McConnell Orthopedic MFG. CO. FDA UDI
Generic Name: Upper-limb traction wrap/trap, single-use FDA UDI
Device Name: Large Hand Wrap (Box of 10) FDA UDI
Model / Reference: 12-215 FDA UDI
Description: Large Hand Wrap (Box of 10) FDA UDI

Identifiers

Catalog Number: 12-215 FDA UDI
Primary DI / UDI-DI: 00860013953560 FDA UDI
FDA Product Code: CCX FDA UDI
GMDN Term: Upper-limb traction wrap/trap, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.6820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Upper-limb traction wrap/trap, single-use

McConnell Orthopedic MFG. CO. by Mcconnell Orthopedic Mfg. Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Mcconnell Orthopedic Mfg. Co.

Sources (1)

FDA UDI e811f132-8504-4e1a-b972-56a4d53782f4 35 fields · synced Jun 6, 2026