Tech-Medical Services

GUDID 10851695005194

Insufflation Tubing, O-ring Connector, Non-Sterile

TECHMEDICAL SERVICES, INC.

Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use Endoscopic insufflation tubing set, single-use

• Primary Device ID: 10851695005194
• NIH Device Record Key: dbccdd21-f801-4717-ad24-c0d8f5df6e56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tech-Medical Services
• Version Model Number: TM102NS
• Company DUNS: 556093219
• Company Name: TECHMEDICAL SERVICES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851695005197 [Primary]
GS1	10851695005194 [Package]; Contains: 00851695005197; Package: Box [50 Units]; In Commercial Distribution

FDA Product Code

• NKC: Tubing/Tubing With Filter, Insufflation, Laparoscopic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

[10851695005194]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-05
• Device Publish Date: 2021-06-26

On-Brand Devices [Tech-Medical Services]

• 10851695005064: Insufflation Tubing, O-Ring Connector
• 10851695005231: Insufflation Tubing, Dual Luer Lock Connectors
• 10851695005224: Insufflation Tubing, Heated with Click-in Funnel Connector
• 00851695005050: Insufflation Tubing, Click-in Funnel Connector
• 00851695005043: Insufflation Tubing, 15/22 Connector
• 10851695005248: Insufflation Tubing, Dual Luer Lock, Non-Sterile
• 10851695005217: Insufflation Tubing, Funnel Connector, Non-Sterile
• 10851695005200: Insufflation Tubing, 15/22 Connector, Non-Sterile
• 10851695005194: Insufflation Tubing, O-ring Connector, Non-Sterile
• 10851695005149: Insufflation Tubing, Heated with 15/22 Connector