Susi

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name: SUSI FDA UDI
Generic Name: Self-retaining surgical retractor, single-use FDA UDI
Device Name: WEITLANER SUSI Retractor (Self Retaining), 5 1/8", (130 mm), 3 x 4 prongs, semi-sharp, sterile, disposable, pack of 20 pcs, single packed FDA UDI
Model / Reference: BV067SU FDA UDI
Description: WEITLANER SUSI Retractor (Self Retaining), 5 1/8", (130 mm), 3 x 4 prongs, semi-sharp, sterile, disposable, pack of 20 pcs, single packed FDA UDI

Identifiers

Catalog Number: BV067SU FDA UDI
Primary DI / UDI-DI: 04046963359515 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Self-retaining surgical retractor, 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

Yes

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

Category: Self-retaining surgical retractor, single-use

Susi by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Endo Retract — Covidien LP · Class I

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: Aesculap, Inc.

Sources (1)

FDA UDI 4cc04f21-6fff-45ff-9f82-6d1e3f9de312 35 fields · synced May 30, 2026