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Birminghamhipresurfacing(bhr)

FDA UDI

Class III (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
BIRMINGHAMHIPRESURFACING(BHR) FDA UDI
Generic Name
General-purpose suction system, vacuum FDA UDI
Device Name
BHR VENTING CANNULA 2.3MM FDA UDI
Model / Reference
999904 FDA UDI
Description
BHR VENTING CANNULA 2.3MM FDA UDI

Identifiers

Catalog Number
999904 FDA UDI
Primary DI / UDI-DI
03596010504609 FDA UDI
PMA Number
P040033 FDA UDI
FDA Product Code
NXT FDA UDI
GMDN Term
General-purpose suction system, vacuum FDA UDI

Classification

Device Class
Class III 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose suction system, vacuum

Birminghamhipresurfacing(bhr) by Smith & Nephew, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose suction system, vacuum.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6f112519-3cbf-4d26-954a-bb4568106e0f 36 fields · synced Jun 8, 2026