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Customed

FDA UDI

Class II (US FDA UDI)

by Customed, Inc.

Identity

Trade Name
CUSTOMED FDA UDI
Generic Name
Cell-block cytology aspiration needle FDA UDI
Device Name
CUSTOMED FRANSEEN BIOPSY FINE ASPIRATION NEEDLE, 21G X 160MM, LIGHT GREEN FDA UDI
Model / Reference
712057839116 FDA UDI
Description
CUSTOMED FRANSEEN BIOPSY FINE ASPIRATION NEEDLE, 21G X 160MM, LIGHT GREEN FDA UDI

Identifiers

Catalog Number
9001802116 FDA UDI
Primary DI / UDI-DI
M20890018021160 FDA UDI
510(k) Number
K092338 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Cell-block cytology aspiration needle 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

Dimensions & Sizes

Size
Length — 160 Millimeter FDA UDI
Needle Gauge — 21 Gauge FDA UDI

Category: Cell-block cytology aspiration needle

Customed by Customed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cell-block cytology aspiration needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Customed, Inc.

Sources (1)

  • FDA UDI 0c6cc458-f1a3-4f32-a18d-3efd396d695e 38 fields · synced May 30, 2026