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BD BBL™ Sensi-Disc™ Zone Interpretation Set

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ Sensi-Disc™ Zone Interpretation Set FDA UDI
Generic Name
Antimicrobial sensitivity disc dispenser IVD FDA UDI
Device Name
Set Sensi-Disc Zone Interpretation FDA UDI
Model / Reference
260639 FDA UDI
Description
Set Sensi-Disc Zone Interpretation FDA UDI

Identifiers

Catalog Number
260639 FDA UDI
Primary DI / UDI-DI
00382902606390 FDA UDI
FDA Product Code
JTN FDA UDI
GMDN Term
Antimicrobial sensitivity disc dispenser 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

BD BBL™ Sensi-Disc™ Zone Interpretation Set 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 90793817-f203-4ea2-b55c-fa2e9cf4737a 37 fields · synced May 30, 2026