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eTRAX™ Needle

FDA UDI

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
eTRAX™ Needle FDA UDI
Generic Name
Soft-tissue biopsy procedure kit, non-medicated FDA UDI
Device Name
Sterile needle, 18GA x 6cm with (7.6 tapered to 3.8 x 147cm) CIV-Flex™ cover for use with CIVCO 18GA needle sensor FDA UDI
Model / Reference
610-1806-01 FDA UDI
Description
Sterile needle, 18GA x 6cm with (7.6 tapered to 3.8 x 147cm) CIV-Flex™ cover for use with CIVCO 18GA needle sensor FDA UDI

Identifiers

Catalog Number
610-1806-01 FDA UDI
Primary DI / UDI-DI
00841436103442 FDA UDI
510(k) Number
K092619 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Soft-tissue biopsy procedure kit, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 6 Centimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI

eTRAX™ Needle by Civco Medical Instruments Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K092619 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Civco Medical Instruments Co., Inc.

Sources (1)

  • FDA UDI 4b51c9af-4ac3-4ee3-912c-c3929e1419b6 39 fields · synced Jun 8, 2026