Sterile Set

FDA UDI

Class II (US FDA UDI)

by Aktormed GmbH

Identity

Trade Name: Sterile Set FDA UDI
Generic Name: Surgical camera holder FDA UDI
Device Name: consisting of - 1x Endoscope clamp (141363) - 1x Universal joint (141362) - 1x Tension sleeve D10 (141339) - 1x Tension sleeve D5 (141365) - 1x Sterilization tray (141357) FDA UDI
Model / Reference: 171907 FDA UDI
Description: consisting of - 1x Endoscope clamp (141363) - 1x Universal joint (141362) - 1x Tension sleeve D10 (141339) - 1x Tension sleeve D5 (141365) - 1x Sterilization tray (141357) FDA UDI

Identifiers

Primary DI / UDI-DI: 04260463849073 FDA UDI
FDA Product Code: NAY FDA UDI
GMDN Term: Surgical camera holder FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical camera holder

Sterile Set by Aktormed GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical camera holder.

TEE Kit — CIVCO MEDICAL INSTRUMENTS CO., INC. · Class I
Accu-Beam — Transamerican Technologies International · Class I
Accu-Beam — Transamerican Technologies International · Class I
Accu-Beam — Transamerican Technologies International · Class I
Accu-Beam — Transamerican Technologies International · Class I
Maestro Couplers, 5mm — Moon Surgical, Inc. · Class I
TEE Kit — CIVCO MEDICAL INSTRUMENTS CO., INC. · Class I
Accu-Beam — Transamerican Technologies International · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Aktormed GmbH

Sources (1)

FDA UDI 98746676-3d2d-4b4f-850d-727656de1b4b 33 fields · synced May 30, 2026