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BD BBL™ Sensi-Disc™ Enoxacin - 10 µg

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ Sensi-Disc™ Enoxacin - 10 µg FDA UDI
Generic Name
Antibacterial susceptibility testing disc IVD FDA UDI
Device Name
BD BBL™ Sensi-Disc™ Enoxacin 10 µg FDA UDI
Model / Reference
231662 FDA UDI
Description
BD BBL™ Sensi-Disc™ Enoxacin 10 µg FDA UDI

Identifiers

Catalog Number
231662 FDA UDI
Primary DI / UDI-DI
30382902316627 FDA UDI
510(k) Number
K923952 FDA UDI
FDA Product Code
JTN FDA UDI
GMDN Term
Antibacterial susceptibility testing disc IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.1620 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

BD BBL™ Sensi-Disc™ Enoxacin - 10 µg by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66f2509f-8ad6-4063-982a-9569750ce0c9 38 fields · synced May 30, 2026