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Vertebris

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
VERTEBRIS FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
PUNCTURE NEEDLE SET 18G WL 250MM PACK=10 PCS, sterile, for single use FDA UDI
Model / Reference
4792802 FDA UDI
Description
PUNCTURE NEEDLE SET 18G WL 250MM PACK=10 PCS, sterile, for single use FDA UDI

Identifiers

Catalog Number
4792.802 FDA UDI
Primary DI / UDI-DI
04055207048764 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.2 Millimeter FDA UDI
Length — 250 Millimeter FDA UDI

Category: Spinal needle, single-use

Vertebris by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI d60b6985-c367-4025-a8f5-d04491742e61 37 fields · synced May 30, 2026