← Back to catalogue

BR Surgical, LLC

FDA UDI

Class I (US FDA UDI)

by Br Surgical Llc

Identity

Trade Name
BR Surgical, LLC FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Device Name
VON EICKEN Malleable Suction Tube, w/olive tip, single-use, Ø 9FR, long curve, WL 8.5cm, 10/box FDA UDI
Model / Reference
BR99-29332 FDA UDI
Description
VON EICKEN Malleable Suction Tube, w/olive tip, single-use, Ø 9FR, long curve, WL 8.5cm, 10/box FDA UDI

Identifiers

Catalog Number
BR99-29332 FDA UDI
Primary DI / UDI-DI
00840183530983 FDA UDI
FDA Product Code
GEA FDA UDI
JOL FDA UDI
JZF FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
880.6740 FDA UDI
874.4420 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, single-use

BR Surgical, LLC by Br Surgical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, 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

Manufacturer
Br Surgical Llc

Sources (1)

  • FDA UDI c9638d76-cfe7-4a7c-8a22-ee58c991f3c0 35 fields · synced Jun 1, 2026