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Hickman

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Hickman FDA UDI
Generic Name
Central venous catheter repair kit FDA UDI
Device Name
External Catheter Segment for Hickman 7F Pediatric Dual-Lumen CV Catheters Repair Kit FDA UDI
Model / Reference
0601760 FDA UDI
Description
External Catheter Segment for Hickman 7F Pediatric Dual-Lumen CV Catheters Repair Kit FDA UDI

Identifiers

Catalog Number
0601760 FDA UDI
Primary DI / UDI-DI
00801741036484 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Central venous catheter repair kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 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

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

Dimensions & Sizes

Size
Catheter Gauge — 7 French FDA UDI

Category: Central venous catheter repair kit

Hickman by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Central venous catheter repair kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI 159bfb3c-80f9-4ba2-aa49-fc074d874ba5 36 fields · synced Jun 9, 2026