← Back to catalogue

Medichoice

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Medichoice FDA UDI
Generic Name
Arthroscopic access cannula, single-use FDA UDI
Device Name
Tray Port Access No Heparin Towel Gloves 10cc Syringes Chloraprep Adhesive Bandage Secureview Blue Towel Mask MediChoice FDA UDI
Model / Reference
PA1008A FDA UDI
Description
Tray Port Access No Heparin Towel Gloves 10cc Syringes Chloraprep Adhesive Bandage Secureview Blue Towel Mask MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632146749 FDA UDI
510(k) Number
K921204 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Arthroscopic access cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arthroscopic access cannula, single-use

Medichoice by Owens & Minor Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic access cannula, single-use.

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 62be786f-b464-4378-8ee6-95a97cf94e3f 35 fields · synced May 30, 2026