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Progel

FDA UDI

Class III (US FDA UDI)

by Neomend, Inc.

Identity

Trade Name
Progel FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
Progel, Pleural Air Leak Sealant, Extended Applicator Spray Tip, 29 cm FDA UDI
Model / Reference
PGEN005-11 FDA UDI
Description
Progel, Pleural Air Leak Sealant, Extended Applicator Spray Tip, 29 cm FDA UDI

Identifiers

Catalog Number
PGEN005-11 FDA UDI
Primary DI / UDI-DI
00801741010019 FDA UDI
FDA Product Code
NBE FDA UDI
GMDN Term
General-purpose absorbent tip applicator/swab, single-use FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 29 Centimeter FDA UDI

Category: General-purpose absorbent tip applicator/swab, single-use

Progel by Neomend, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neomend, Inc.

Sources (1)

  • FDA UDI 5dcb9ca9-7b8e-4bc8-926e-bf3121ee244a 36 fields · synced Jun 8, 2026