← Back to catalogue

Pediatric plunger

FDA UDI

Class II (US FDA UDI)

by Efer Endoscopy

Identity

Trade Name
Pediatric plunger FDA UDI
Generic Name
Rigid optical bronchoscope FDA UDI
Device Name
Pediatric plunger, color coded black FDA UDI
Model / Reference
BP2402-3 FDA UDI
Description
Pediatric plunger, color coded black FDA UDI

Identifiers

Primary DI / UDI-DI
03700620600419 FDA UDI
510(k) Number
K854414 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 plunger by Efer Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical bronchoscope.

Cleared under the same submission

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

Manufacturer
Efer Endoscopy

Sources (1)

  • FDA UDI 4df5f83e-1dda-49b0-b961-0358ed70b994 34 fields · synced May 31, 2026