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Epidural Anesthesia Kit

FDA UDI

Class II (US FDA UDI)

by Custom Interventional Pain Management

Identity

Trade Name
Epidural Anesthesia Kit FDA UDI
Generic Name
Epidural anaesthesia set, medicated FDA UDI
Device Name
Convenience kit with Lidocaine FDA UDI
Model / Reference
17LID FDA UDI
Description
Convenience kit with Lidocaine FDA UDI

Identifiers

Catalog Number
17LID FDA UDI
Primary DI / UDI-DI
B87517LID0 FDA UDI
FDA Product Code
OGE FDA UDI
GMDN Term
Epidural anaesthesia set, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Epidural anaesthesia set, medicated

Epidural Anesthesia Kit by Custom Interventional Pain Management — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Epidural anaesthesia set, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Custom Interventional Pain Management

Sources (1)

  • FDA UDI f43aa6a2-b2c6-4d4d-9cbb-8a870a7c0b52 34 fields · synced May 30, 2026