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BiomarC ®

FDA UDI

Class II (US FDA UDI)

by Carbon Medical Technologies, Inc.

Identity

Trade Name
BiomarC ® FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Device Name
Coaxial Needle FDA UDI
Model / Reference
040143 FDA UDI
Description
Coaxial Needle FDA UDI

Identifiers

Catalog Number
040143 FDA UDI
Primary DI / UDI-DI
00858015005646 FDA UDI
510(k) Number
K133148 FDA UDI
FDA Product Code
NEU FDA UDI
FBK FDA UDI
GMDN Term
Needle guide, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 FDA UDI
876.1500 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 8.5 Centimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: Needle guide, single-use

BiomarC ® by Carbon Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2aa4331d-eb10-4e9a-b525-c4c449d487b1 37 fields · synced Jun 9, 2026