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Adaptor

FDA UDI

Class II (US FDA UDI)

by Sapi Med Spa

Identity

Trade Name
Adaptor FDA UDI
Generic Name
Light source adaptor FDA UDI
Device Name
Autoclavable teflon cable-end to connect Wolf/Storz cables to fit Sapimed's Self-Light grips. FDA UDI
Model / Reference
Fiber cable adaptor FDA UDI
Description
Autoclavable teflon cable-end to connect Wolf/Storz cables to fit Sapimed's Self-Light grips. FDA UDI

Identifiers

Catalog Number
B.0365 FDA UDI
Primary DI / UDI-DI
08033638801192 FDA UDI
FDA Product Code
FER FDA UDI
GMDN Term
Light source adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Light source adaptor

Adaptor by Sapi Med Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Light source adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sapi Med Spa

Sources (1)

  • FDA UDI 5fc955b7-87d6-4071-8bb3-12b2aad838fd 34 fields · synced May 31, 2026