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Safetrap Tissue Collector

FDA UDI

Class II (US FDA UDI)

by Oto-Med, Inc.

Identity

Trade Name
SAFETRAP TISSUE COLLECTOR FDA UDI
Generic Name
General specimen container IVD, no additive, sterile FDA UDI
Device Name
SAFETRAP TISSUE COLLECTOR FDA UDI
Model / Reference
SP-2000 FDA UDI
Description
SAFETRAP TISSUE COLLECTOR FDA UDI

Identifiers

Primary DI / UDI-DI
00850000126107 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
General specimen container IVD, no additive, sterile 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

Yes

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

No

FDA UDI

Category: General specimen container IVD, no additive, sterile

Safetrap Tissue Collector by Oto-Med, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oto-Med, Inc.

Sources (1)

  • FDA UDI b27f80b8-8ca1-46af-b3dd-dd44b5d1f205 34 fields · synced Jun 8, 2026