Lccs

FDA UDI

Class II (US FDA UDI)

by Lccs Products Limited

Identity

Trade Name: LCCS FDA UDI
Generic Name: Spinal needle, single-use FDA UDI
Device Name: AN-SI SPINAL NEEDLE FDA UDI
Model / Reference: SQ20113-LC FDA UDI
Description: AN-SI SPINAL NEEDLE FDA UDI

Identifiers

Primary DI / UDI-DI: 04895233606725 FDA UDI
510(k) Number: K131006 FDA UDI
FDA Product Code: BSP FDA UDI
GMDN Term: Spinal needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5150 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Spinal needle, single-use

Lccs by Lccs Products Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Spinal needle, single-use.

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Spinocan® — B. BRAUN MEDICAL INC. · Class II
Temena — Te ME NA Sas · Class II

Cleared under the same submission

K131006 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Lccs Products Limited

Sources (1)

FDA UDI c272f980-193b-4b67-9b66-64d7d8919f07 35 fields · synced Jun 8, 2026