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Pos-T-Vac

FDA UDI

by Pos-T-Vac LLC

Identity

Trade Name
Pos-T-Vac FDA UDI
Generic Name
Penile vacuum device FDA UDI
Model / Reference
PTV Manual 3000/MOS System FDA UDI

Identifiers

Catalog Number
V113 FDA UDI
Primary DI / UDI-DI
00656535000918 FDA UDI
GMDN Term
Penile vacuum device FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Penile vacuum device

Pos-T-Vac by Pos-T-Vac LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Penile vacuum device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pos-T-Vac LLC

Sources (1)

  • FDA UDI 23cffb4d-52c5-4510-a3b4-047431b2ab1d 33 fields · synced Jun 1, 2026