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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
Corneal marker, single-use FDA UDI
Device Name
d'assumpcao face lift marker, 8.0 mm wide, 6" (15.2 cm), w/ ratchet FDA UDI
Model / Reference
E7940-26 FDA UDI
Description
d'assumpcao face lift marker, 8.0 mm wide, 6" (15.2 cm), w/ ratchet FDA UDI

Identifiers

Catalog Number
E7940-26 FDA UDI
Primary DI / UDI-DI
00842331186578 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Corneal marker, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 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: Corneal marker, single-use

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

Similar devices

Also classified as Corneal marker, single-use.

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 c8e275f2-e1b8-4cff-9bb5-1e6f3785c6cc 35 fields · synced Jun 1, 2026