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Jigsaw Medical, LLC

FDA UDI

Class I (US FDA UDI)

by Jigsaw Medical, Llc

Identity

Trade Name
Jigsaw Medical,LLC FDA UDI
Generic Name
Luer/epidural catheter linear connector FDA UDI
Device Name
Needleless Injection Site, Swabbable Female Luer Lock, Male Luer Lock FDA UDI
Model / Reference
80150 FDA UDI
Description
Needleless Injection Site, Swabbable Female Luer Lock, Male Luer Lock FDA UDI

Identifiers

Primary DI / UDI-DI
00856274008590 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Luer/epidural catheter linear connector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer/epidural catheter linear connector

Jigsaw Medical, LLC by Jigsaw Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer/epidural catheter linear connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jigsaw Medical, Llc

Sources (1)

  • FDA UDI 3b49d38a-ad7b-401a-ac0e-3e70f61c91ad 33 fields · synced Jun 8, 2026