← Back to catalogue

Resp-O2 Mucus Specimen Trap, Leak Proof Transport Cap, 40 cc, Sterile

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Mucus Specimen Trap, Leak Proof Transport Cap, 40 cc, Sterile FDA UDI
Generic Name
Oropharyngeal secretion specimen suction kit FDA UDI
Model / Reference
32270 FDA UDI

Identifiers

Primary DI / UDI-DI
00840117310377 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
Oropharyngeal secretion specimen suction kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oropharyngeal secretion specimen suction kit

Resp-O2 Mucus Specimen Trap, Leak Proof Transport Cap, 40 cc, Sterile by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oropharyngeal secretion specimen suction kit.

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
Dynarex Corp.

Sources (1)

  • FDA UDI 03613e79-01c1-40cb-8698-c1870b557619 32 fields · synced May 31, 2026