Identity
- Trade Name
- APA™ MIL Camera Module(L) FDA UDI
- Generic Name
- Rigid intubation laryngoscope, reusable FDA UDI
- Device Name
- The APA™ Video Laryngoscope is a multi-functional device designed to assist direct and indirect laryngoscopy in routine and difficult airway intubations. It may be used to facilitate endotracheal intubation as part of general anaesthesia or CPR (cardiopulmonary resuscitation) during cardiac arrest. The video laryngoscope is reusable, DEHP-free and latex-free. It is fully detachable into three components: APA™ Video Viewer, APA™ Handle and APA™ MAC or MIL Camera Module(Small and Large size). When used as a standard laryngoscope, the appropriate Camera Module is attached to the Handle to obtain a view of the laryngeal inlet during endotracheal intubation. When used as a video laryngoscope, the Video Viewer is attached to the Handle and Camera Module to provide improved visualisation during laryngoscopy and endotracheal intubation. FDA UDI
- Model / Reference
- 702930 FDA UDI
- Description
- The APA™ Video Laryngoscope is a multi-functional device designed to assist direct and indirect laryngoscopy in routine and difficult airway intubations. It may be used to facilitate endotracheal intubation as part of general anaesthesia or CPR (cardiopulmonary resuscitation) during cardiac arrest. The video laryngoscope is reusable, DEHP-free and latex-free. It is fully detachable into three components: APA™ Video Viewer, APA™ Handle and APA™ MAC or MIL Camera Module(Small and Large size). When used as a standard laryngoscope, the appropriate Camera Module is attached to the Handle to obtain a view of the laryngeal inlet during endotracheal intubation. When used as a video laryngoscope, the Video Viewer is attached to the Handle and Camera Module to provide improved visualisation during laryngoscopy and endotracheal intubation. FDA UDI
Identifiers
- Catalog Number
- 702930 FDA UDI
- Primary DI / UDI-DI
- 08885009190233 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Rigid intubation laryngoscope, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Rigid intubation laryngoscope, reusable
APA™ MIL Camera Module(L) by Venner Medical (singapore) Pte. Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid intubation laryngoscope, reusable.
- AincA® — Anesthesia Associates, Inc. · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- Reusable Conventional Box Set Mini & Standard Rough Handle + Blades Mac 1, 2, 3, — FLEXICARE MEDICAL LIMITED · Class I
- Propper Miller Fiber Optic Laryngoscope Blade #1 — Propper Manufacturing Co., Inc. · Class I
- AincA® — Anesthesia Associates, Inc. · Class I
- Grafco — GF Health Products, Inc · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- ri-modul set Macintosh baby LED 3.5 V with AA-hand — Rudolf Riester GmbH & Co. KG · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Venner Medical (singapore) Pte. Ltd.
Sources (1)
- FDA UDI afcaae1d-a050-4e20-95e7-faf7a0704284 34 fields · synced Jun 8, 2026