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Maestro Couplers, 10mm

FDA UDIEUDAMED

Class I (US FDA UDI)

by Moon Surgical, Inc.

Identity

Trade Name
Maestro Couplers, 10mm FDA UDI
Generic Name
Surgical camera holder FDA UDI
Model / Reference
201 FDA UDI

Identifiers

Primary DI / UDI-DI
03770025849072 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, 10mm by Moon Surgical, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical camera holder.

Cleared under the same submission

K240598 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moon Surgical, Inc.

Sources (2)

  • FDA UDI 52ff59c9-0fba-4923-875d-aeb2ba13436f 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026