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Bioteque Taiwan Ltd.

FDA UDI

Class II (US FDA UDI)

by Bioteque Taiwan Ltd.

Identity

Trade Name
Bioteque Taiwan Ltd. FDA UDI
Generic Name
Vaginal dilator FDA UDI
Model / Reference
DT-B/S FDA UDI

Identifiers

Primary DI / UDI-DI
04719894432250 FDA UDI
510(k) Number
K130273 FDA UDI
FDA Product Code
HDX FDA UDI
GMDN Term
Vaginal dilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.3900 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

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

Yes

FDA UDI

Category: Vaginal dilator

Bioteque Taiwan Ltd. by Bioteque Taiwan Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal dilator.

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 187cb790-f50b-4ecf-a820-a21400a5373d 33 fields · synced May 30, 2026