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Prosurg

FDA UDI

Class II (US FDA UDI)

by Prosurg, Inc

Identity

Trade Name
Prosurg FDA UDI
Generic Name
Rigid optical arthroscope, single-use FDA UDI
Device Name
Neo-Arthroscope 4.0 mm (30 Degrees) FDA UDI
Model / Reference
NAR40 FDA UDI
Description
Neo-Arthroscope 4.0 mm (30 Degrees) FDA UDI

Identifiers

Catalog Number
NAR40 FDA UDI
Primary DI / UDI-DI
00851545007715 FDA UDI
510(k) Number
K152511 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Rigid optical arthroscope, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Rigid optical arthroscope, single-use

Prosurg by Prosurg, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical arthroscope, single-use.

Cleared under the same submission

K152511 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Prosurg, Inc

Sources (1)

  • FDA UDI 6f47a2fc-eee1-4ac3-bd7e-2bce89d567e0 36 fields · synced May 30, 2026