← Back to catalogue

Discography Kit

FDA UDI

Class II (US FDA UDI)

by Custom Interventional Pain Management

Identity

Trade Name
Discography Kit FDA UDI
Generic Name
Epidural anaesthesia set, medicated FDA UDI
Device Name
Convenience kit containing Lidocaine FDA UDI
Model / Reference
55LID FDA UDI
Description
Convenience kit containing Lidocaine FDA UDI

Identifiers

Catalog Number
55LID FDA UDI
Primary DI / UDI-DI
B87555LID0 FDA UDI
FDA Product Code
OIL FDA UDI
GMDN Term
Epidural anaesthesia set, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1730 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

Discography 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Custom Interventional Pain Management

Sources (1)

  • FDA UDI 113a2f3b-7007-4971-a583-9e1d1f3ca915 34 fields · synced Jun 1, 2026