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C60100

FDA UDI

Class II (US FDA UDI)

by B&B Company Co., Ltd.

Identity

Trade Name
C60100 FDA UDI
Generic Name
Cervical cytology brush FDA UDI
Model / Reference
C60100 100P FDA UDI

Identifiers

Primary DI / UDI-DI
08809157488530 FDA UDI
FDA Product Code
HHT FDA UDI
GMDN Term
Cervical cytology brush FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cervical cytology brush

C60100 by B&B Company Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical cytology brush.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 349f4fa1-2da9-4082-ba3b-c3d63f46705f 32 fields · synced Jun 6, 2026