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Midwest Medical Inc. (Private Label)

FDA UDI

Class II (US FDA UDI)

by Manan Medical Products, Inc.

Identity

Trade Name
Midwest Medical Inc. (Private Label) FDA UDI
Generic Name
Soft-tissue biopsy needle, single-use FDA UDI
Device Name
22 GA x 15CM MARKED CHIBA NEEDLE FDA UDI
Model / Reference
CNM2206-MM FDA UDI
Description
22 GA x 15CM MARKED CHIBA NEEDLE FDA UDI

Identifiers

Catalog Number
CNM2206-MM FDA UDI
Primary DI / UDI-DI
00859013006048 FDA UDI
510(k) Number
K851838 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Soft-tissue biopsy needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 15 Centimeter FDA UDI

Category: Soft-tissue biopsy needle, single-use

Midwest Medical Inc. (Private Label) by Manan Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue biopsy needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7563c5c-9487-467a-9ee7-adc5bb663861 37 fields · synced Jun 1, 2026