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Bebe Vie

FDA UDI

Class I (US FDA UDI)

by Adroit Surgical LLC

Identity

Trade Name
Bebe Vie FDA UDI
Generic Name
Rigid intubation laryngoscope, single-use FDA UDI
Device Name
The Bebe Vie is a single-use pediatric laryngoscope for intubation of toddlers to age ten. FDA UDI
Model / Reference
BB-111 FDA UDI
Description
The Bebe Vie is a single-use pediatric laryngoscope for intubation of toddlers to age ten. FDA UDI

Identifiers

Primary DI / UDI-DI
00860115000612 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

Bebe Vie 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adroit Surgical LLC

Sources (1)

  • FDA UDI 0e3d7b4a-35c7-410b-bd58-86d95dd201fd 33 fields · synced Sep 17, 2026