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: Arm procedure positioner, reusable FDA UDI
Device Name: Articulated Sterile Intraoperative Positioner - Comprised of 2-400 Support Frame, 3-200 Control Tube, 7-200 UEP Accessory, EC-302 Equipment Cart, and 12-401EV Large Arm Support Wrap (Complimentary Box of 4) FDA UDI
Model / Reference: ASIP #120 FDA UDI
Description: Articulated Sterile Intraoperative Positioner - Comprised of 2-400 Support Frame, 3-200 Control Tube, 7-200 UEP Accessory, EC-302 Equipment Cart, and 12-401EV Large Arm Support Wrap (Complimentary Box of 4) FDA UDI

Identifiers

Catalog Number: ASIP #120 FDA UDI
Primary DI / UDI-DI: 00860013953508 FDA UDI
FDA Product Code: BWN FDA UDI
GMDN Term: Arm procedure positioner, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4950 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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Contains Latex

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Prescription Use

Yes

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Over-the-Counter

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Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

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Premarket Exempt

Yes

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Lot / Batch Number

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Serial Number

Yes

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Arm procedure positioner, reusable

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 db0e76ea-fce8-4446-b55e-03153f9b85e1 35 fields · synced May 30, 2026