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Td-5®

FDA UDI

Class II (US FDA UDI)

by Cs Medical Llc

Identity

Trade Name
TD-5® FDA UDI
Generic Name
Glutaraldehyde device sterilant FDA UDI
Device Name
TD-5® High Level Disinfectant FDA UDI
Model / Reference
TD-5 FDA UDI
Description
TD-5® High Level Disinfectant FDA UDI

Identifiers

Catalog Number
CS-TD-5 FDA UDI
Primary DI / UDI-DI
B205TD5A1 FDA UDI
510(k) Number
K051305 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Glutaraldehyde device sterilant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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

Yes

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

No

FDA UDI

Category: Glutaraldehyde device sterilant

Td-5® by Cs Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glutaraldehyde device sterilant.

Cleared under the same submission

K051305 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cs Medical Llc

Sources (1)

  • FDA UDI 96b43b16-4281-45e0-b034-50fff67a6ce4 37 fields · synced Jun 6, 2026