Vertebris

FDA UDI

Class I (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 90MM PACK=10 PCS, sterile, for single use FDA UDI
Model / Reference: 492206112 FDA UDI
Description: PUNCTURE NEEDLE SET 18G WL 90MM PACK=10 PCS, sterile, for single use FDA UDI

Identifiers

Catalog Number: 492206112 FDA UDI
Primary DI / UDI-DI: 04055207049174 FDA UDI
FDA Product Code: GEA FDA UDI
GMDN Term: Spinal needle, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 90 Millimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: Spinal needle, single-use

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

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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 I	Pending data

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Manufacturer

Manufacturer: Richard Wolf GmbH

Sources (1)

FDA UDI 7288977d-7b33-4a18-9dad-f6a0fc2ceca2 37 fields · synced Jun 8, 2026