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Tech Medical Services

FDA UDI

Class II (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
Curved Universal Wireless Probe Cover with Probe Cradle FDA UDI
Model / Reference
TMPH-2005 FDA UDI
Description
Curved Universal Wireless Probe Cover with Probe Cradle FDA UDI

Identifiers

Primary DI / UDI-DI
00851695005593 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Instrument/equipment drape, single-use, sterile 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

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 II — 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 13dfa47a-e3f0-4c9f-a378-93f5b7aa6d1f 33 fields · synced May 30, 2026