Gertie Marx Spinal N

FDA UDI

Class II (US FDA UDI)

by International Medical Development Corporation

Identity

Trade Name: GERTIE MARX SPINAL N FDA UDI
Generic Name: Spinal needle, single-use FDA UDI
Device Name: EPIDURAL NEEDLE FDA UDI
Model / Reference: FNB2090-I-8 FDA UDI
Description: EPIDURAL NEEDLE FDA UDI

Identifiers

Primary DI / UDI-DI: B274FNB2090I80 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Spinal needle, single-use

Gertie Marx Spinal N by International Medical Development Corporation — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: International Medical Development Corporation

Sources (1)

FDA UDI 6cd2f2be-96f4-440a-aeff-95f3e892b7f7 33 fields · synced May 31, 2026