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Tech Medical Services

FDA UDI

Class I (US FDA UDI)

by Tech Medical Services, Inc.

Identity

Trade Name
Tech Medical Services FDA UDI
Generic Name
Instrument/equipment drape, single-use, sterile FDA UDI
Device Name
Probe Cover with Probe Holder and Probe Battery Included FDA UDI
Model / Reference
TMPH-2006 FDA UDI
Description
Probe Cover with Probe Holder and Probe Battery Included FDA UDI

Identifiers

Primary DI / UDI-DI
00851695005609 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Instrument/equipment drape, single-use, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Instrument/equipment drape, single-use, sterile

Tech Medical Services by Tech Medical Services, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tech Medical Services, Inc.

Sources (1)

  • FDA UDI 1370069f-1492-43d4-a3a9-3942702beeec 33 fields · synced May 30, 2026