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Epimed International, Inc.

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 125-2060TModel Epidural Introducer Needle

by Epimed International, Inc.

Identity

Trade Name
Epimed International,Inc. EUDAMED
Epimed FDA UDI
Generic Name
Epidural needle, non-threaded FDA UDI
Device Name
20g TW x 6.0" Tuohy Epidural Needle FDA UDI
Model / Reference
Epidural Introducer Needle EUDAMED
125-2060T EUDAMEDFDA UDI
Description
20g TW x 6.0" Tuohy Epidural Needle FDA UDI

Identifiers

Catalog Number
125-2060T FDA UDI
Primary DI / UDI-DI
00818788020840 EUDAMEDFDA UDI
Basic UDI-DI
081878802EINL2 EUDAMED
510(k) Number
K030562 FDA UDI
FDA Product Code
BSP FDA UDI
EMDN Code
A01030102 EPIDURAL ANAESTHESIA NEEDLES AND KITS EUDAMED
GMDN Term
Epidural needle, non-threaded FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.5150 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 20 Gauge FDA UDI
Length — 6 Inch FDA UDI

Epimed International, Inc. by Epimed International, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000010774
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 72f136cd-3e66-4472-bdb8-6d0f334f6a86 61 fields · synced Jun 8, 2026
  • FDA UDI 9de44550-c7ff-4a81-8e34-22b54df0c9e6 38 fields · synced May 30, 2026