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AincA®

FDA UDI

Class I (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name
AincA® FDA UDI
Generic Name
Flexible intubation laryngoscope, video, reusable FDA UDI
Device Name
VideoStylet (Only), Model "C" stylet (Length = 34.5cm / 13.6", Nominal 8.0 to 8.5mm ETT). FDA UDI
Model / Reference
00-675-C-1 FDA UDI
Description
VideoStylet (Only), Model "C" stylet (Length = 34.5cm / 13.6", Nominal 8.0 to 8.5mm ETT). FDA UDI

Identifiers

Catalog Number
00-675-C-1 FDA UDI
Primary DI / UDI-DI
B00500675C10 FDA UDI
FDA Product Code
CAL FDA UDI
GMDN Term
Flexible intubation laryngoscope, video, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5530 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

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: Flexible intubation laryngoscope, video, reusable

AincA® by Anesthesia Associates, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible intubation laryngoscope, video, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anesthesia Associates, Inc.

Sources (1)

  • FDA UDI a8f5c846-7edc-471b-a3a9-504aaed8a24e 35 fields · synced May 31, 2026