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Novo Surgical Inc.

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name
Novo Surgical Inc. FDA UDI
Generic Name
Rib spreader, reusable FDA UDI
Device Name
balfour abdominal retractor w/ fixed side blades, w/ ratchet bar mechanism, w/ fixed fenestrated side blades, 7 1/8" (18.1 cm) maximum spread, side blades 4" deep & center blade #2470-73 (3 3/8" x 2 1/2") FDA UDI
Model / Reference
G3581-26R FDA UDI
Description
balfour abdominal retractor w/ fixed side blades, w/ ratchet bar mechanism, w/ fixed fenestrated side blades, 7 1/8" (18.1 cm) maximum spread, side blades 4" deep & center blade #2470-73 (3 3/8" x 2 1/2") FDA UDI

Identifiers

Catalog Number
G3581-26R FDA UDI
Primary DI / UDI-DI
00842331165740 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Rib spreader, reusable 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

No

FDA UDI

Single Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rib spreader, reusable

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

Similar devices

Also classified as Rib spreader, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novo Surgical, Inc.

Sources (1)

  • FDA UDI f61d40ef-a649-450b-be74-ab8f6f3bdff3 35 fields · synced May 30, 2026