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Temena

FDA UDI

Class II (US FDA UDI)

by Te ME NA Sas

Identity

Trade Name
Temena FDA UDI
Generic Name
Anaesthesia conduction catheter FDA UDI
Device Name
Epidural catheter 20G x 900 mm with stylet FDA UDI
Model / Reference
03590M20 FDA UDI
Description
Epidural catheter 20G x 900 mm with stylet FDA UDI

Identifiers

Catalog Number
03590M20 FDA UDI
Primary DI / UDI-DI
03700339710324 FDA UDI
FDA Product Code
BSO FDA UDI
GMDN Term
Anaesthesia conduction catheter 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

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
Length — 900 Millimeter FDA UDI
Catheter Gauge — 2.7 French FDA UDI

Category: Anaesthesia conduction catheter

Temena by Te ME NA Sas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia conduction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Te ME NA Sas

Sources (1)

  • FDA UDI 89d3b871-ed8b-4b69-9b6b-1c39a724859a 35 fields · synced May 30, 2026