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Scintillant

FDA UDI

Class II (US FDA UDI)

by BihlerMed, L.L.C.

Identity

Trade Name
Scintillant FDA UDI
Generic Name
Suction cannula, single-use FDA UDI
Device Name
Scintillant Surgical Light with Suction FDA UDI
Model / Reference
2658-01-0002 FDA UDI
Description
Scintillant Surgical Light with Suction FDA UDI

Identifiers

Primary DI / UDI-DI
10865082000129 FDA UDI
FDA Product Code
JOL FDA UDI
FTD FDA UDI
GMDN Term
Suction cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
878.4580 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Category: Operating room lightSuction cannula, single-use

Scintillant by BihlerMed, L.L.C. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BihlerMed, L.L.C.

Sources (1)

  • FDA UDI b49fef6a-add5-4c3b-9f2d-69f7c998fb7b 34 fields · synced May 29, 2026