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Pediatric base

FDA UDI

Class II (US FDA UDI)

by Efer Endoscopy

Identity

Trade Name
Pediatric base FDA UDI
Generic Name
Rigid optical bronchoscope FDA UDI
Device Name
Pediatric base with BB2403-3 jet ventilation obturator FDA UDI
Model / Reference
BD2301-3 FDA UDI
Description
Pediatric base with BB2403-3 jet ventilation obturator FDA UDI

Identifiers

Primary DI / UDI-DI
03700620600754 FDA UDI
FDA Product Code
EOQ FDA UDI
GMDN Term
Rigid optical bronchoscope 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical bronchoscope

Pediatric base by Efer Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical bronchoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Efer Endoscopy

Sources (1)

  • FDA UDI be94a6d6-10f5-4481-b539-46b1f433a657 33 fields · synced Jun 6, 2026