Identity
- Trade Name
- Vie Scope FDA UDI
- Generic Name
- Rigid intubation laryngoscope, single-use FDA UDI
- Device Name
- The Vie Scope is a single-use intubation device whose transparent polymer tubing and LED lights allow for an enhanced line of sight. FDA UDI
- Model / Reference
- VS-103 FDA UDI
- Description
- The Vie Scope is a single-use intubation device whose transparent polymer tubing and LED lights allow for an enhanced line of sight. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860115000605 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Rigid intubation laryngoscope, single-use 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
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Rigid intubation laryngoscope, single-use
Vie Scope by Adroit Surgical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid intubation laryngoscope, single-use.
- Curaplex — BOUND TREE MEDICAL, LLC · Class I
- BritePro Solo Single-Use Fiber Optic Handle and Blade Phillips 2 — FLEXICARE MEDICAL LIMITED · Class I
- Carnegie Surgical LLC — Carnegie Surgical LLC · Class I
- Carnegie Surgical LLC — Carnegie Surgical LLC · Class I
- MedSource Disposable Laryngoscope Blade — MEDSOURCE INTERNATIONAL LLC · Class I
- BritePro Solo Single-Use Fiber Optic Handle and Blade Miller 3 — FLEXICARE MEDICAL LIMITED · Class I
- MedSource Disposable Laryngoscope Set — MEDSOURCE INTERNATIONAL LLC · Class I
- MedSource Disposable Laryngoscope Blade — MEDSOURCE INTERNATIONAL LLC · 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
- Adroit Surgical LLC
Sources (1)
- FDA UDI f121c77e-a4dd-4efb-a010-85fe072bb136 33 fields · synced Sep 17, 2026