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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
Endoscopic insufflation tubing set, single-use FDA UDI
Device Name
Insufflation Tubing, Dual Luer Lock, Non-Sterile FDA UDI
Model / Reference
TMITF10NS FDA UDI
Description
Insufflation Tubing, Dual Luer Lock, Non-Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00851695005241 FDA UDI
FDA Product Code
NKC FDA UDI
GMDN Term
Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1730 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

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: Endoscopic insufflation tubing set, single-use

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 Endoscopic insufflation tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 09027554-99b0-470a-adab-878012281e72 33 fields · synced May 31, 2026