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Tsi

FDA UDI

Class I (US FDA UDI)

by Tedan Surgical Innovations, L.l.c.

Identity

Trade Name
TSI FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Device Name
LIGHT CABLE, 10', STERILE, 5/BOX FDA UDI
Model / Reference
ML-0046 FDA UDI
Description
LIGHT CABLE, 10', STERILE, 5/BOX FDA UDI

Identifiers

Primary DI / UDI-DI
00851797006504 FDA UDI
FDA Product Code
FDG FDA UDI
GMDN Term
Electrical-only medical device connection cable, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4530 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical-only medical device connection cable, single-use

Tsi by Tedan Surgical Innovations, L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5fecfd58-b6a9-4924-a788-1aebe775084c 33 fields · synced Jun 8, 2026