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Discseel

FDA UDI

Class II (US FDA UDI)

by Custom Interventional Pain Management

Identity

Trade Name
Discseel FDA UDI
Generic Name
Intrathecal anaesthesia set, medicated FDA UDI
Device Name
Convenience kit with Lidocaine FDA UDI
Model / Reference
DSCLID FDA UDI
Description
Convenience kit with Lidocaine FDA UDI

Identifiers

Catalog Number
DSCLID FDA UDI
Primary DI / UDI-DI
B875DSCLID0 FDA UDI
FDA Product Code
OFU FDA UDI
GMDN Term
Intrathecal 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: Intrathecal anaesthesia set, medicated

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

Similar devices

Also classified as Intrathecal 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 dce6d1f2-4a01-483d-bae9-43043b914424 34 fields · synced Jun 8, 2026