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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
Tenotome FDA UDI
Device Name
micro scissors, round handle, dissecting, handle 7.0 mm diameter, curved blade 11.0 mm long for fine dissection, 12.0 cm FDA UDI
Model / Reference
78SDC-12R7 FDA UDI
Description
micro scissors, round handle, dissecting, handle 7.0 mm diameter, curved blade 11.0 mm long for fine dissection, 12.0 cm FDA UDI

Identifiers

Catalog Number
78SDC-12R7 FDA UDI
Primary DI / UDI-DI
00842331158094 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Tenotome 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: Tenotome

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

Similar devices

Also classified as Tenotome.

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 3c8b8c0e-cf26-4398-a5d3-c4fa73539dd0 35 fields · synced Jun 8, 2026