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Maestro Couplers, 5mm

FDA UDI

Class I (US FDA UDI)

by Moon Surgical, Inc.

Identity

Trade Name
Maestro Couplers, 5mm FDA UDI
Generic Name
Surgical camera holder FDA UDI
Model / Reference
200 FDA UDI

Identifiers

Primary DI / UDI-DI
03770025849089 FDA UDI
510(k) Number
K240598 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
Surgical camera holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical camera holder

Maestro Couplers, 5mm by Moon Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical camera holder.

Cleared under the same submission

K240598 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moon Surgical, Inc.

Sources (1)

  • FDA UDI 9d4accba-56fb-4b26-b531-62059087e434 34 fields · synced May 30, 2026