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AtriCure SI Retractor Blade

FDA UDI

Class I (US FDA UDI)

by Atricure, Inc.

Identity

Trade Name
AtriCure SI Retractor Blade FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
SI Retractor Blade, 40mm W X 30mm L, Slim FDA UDI
Model / Reference
001-400-181 FDA UDI
Description
SI Retractor Blade, 40mm W X 30mm L, Slim FDA UDI

Identifiers

Primary DI / UDI-DI
00818354014013 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 30 Millimeter FDA UDI
Width — 40 Millimeter FDA UDI

Category: Surgical retractor/retraction system blade, reusable

AtriCure SI Retractor Blade by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atricure, Inc.

Sources (1)

  • FDA UDI 9a8f39cc-ae4a-4090-b93e-86bd0c2d3724 35 fields · synced Jun 8, 2026