← Back to catalogue

Procure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
Procure FDA UDI
Generic Name
Oesophageal-obturating/tracheal airway, single-use FDA UDI
Device Name
Standard Berman Oral Airway 100mm (Individually Bagged) FDA UDI
Model / Reference
1002266 FDA UDI
Description
Standard Berman Oral Airway 100mm (Individually Bagged) FDA UDI

Identifiers

Catalog Number
1002266 FDA UDI
Primary DI / UDI-DI
10840330700648 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Oesophageal-obturating/tracheal airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5110 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oesophageal-obturating/tracheal airway, single-use

Procure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oesophageal-obturating/tracheal airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI 85bc9da7-c0c8-4efa-9812-d63d1a0df12f 35 fields · synced May 31, 2026