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JetPeel

FDA UDI

Class I (US FDA UDI)

by Tav - Tech Ltd

Identity

Trade Name
JetPeel FDA UDI
Generic Name
Liquid-jet skin surface treatment system applicator, single-use FDA UDI
Model / Reference
JetPeel Tubing FDA UDI

Identifiers

Catalog Number
JTO-003 FDA UDI
Primary DI / UDI-DI
07290014242357 FDA UDI
FDA Product Code
GFE FDA UDI
GMDN Term
Liquid-jet skin surface treatment system applicator, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

FDA UDI

Over-the-Counter

Yes

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: Liquid-jet skin surface treatment system applicator, single-use

JetPeel by Tav - Tech Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liquid-jet skin surface treatment system applicator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tav - Tech Ltd

Sources (1)

  • FDA UDI 97396814-2afd-47b5-9456-a131ee835330 34 fields · synced Jun 1, 2026