← Back to catalogue

Innovex

FDA UDI

Class II (US FDA UDI)

by Shanghai Anqing Medical Instrument Co., Ltd

Identity

Trade Name
Innovex FDA UDI
Generic Name
Flexible video bronchoscope, single-use FDA UDI
Model / Reference
BS59H-28EU FDA UDI

Identifiers

Primary DI / UDI-DI
06970034210444 FDA UDI
FDA Product Code
EOQ FDA UDI
GMDN Term
Flexible video bronchoscope, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible video bronchoscope, single-use

Innovex by Shanghai Anqing Medical Instrument Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video bronchoscope, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 473df7cb-2e9d-45f0-925a-f5378d558664 32 fields · synced May 30, 2026