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Preat

FDA UDI

Class I (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Preat FDA UDI
Generic Name
Resilient dental precision attachment FDA UDI
Device Name
O-Ring Mini Implant Servicing Kit. kit contains . 2 O-Ring Black Rings #2 Micro Single . 1 O-Ring Yellow Processing #2 Micro Single . 1 O-Ring Purple Rings MH-2 Extra Strong Single. 1 O-Ring Closed Metal Housing #2 MH-2. 1 O-Ring Mini Implant Analog. 1 O-Ring Mini Implant Impression Coping FDA UDI
Model / Reference
1500610 FDA UDI
Description
O-Ring Mini Implant Servicing Kit. kit contains . 2 O-Ring Black Rings #2 Micro Single . 1 O-Ring Yellow Processing #2 Micro Single . 1 O-Ring Purple Rings MH-2 Extra Strong Single. 1 O-Ring Closed Metal Housing #2 MH-2. 1 O-Ring Mini Implant Analog. 1 O-Ring Mini Implant Impression Coping FDA UDI

Identifiers

Catalog Number
1500610 FDA UDI
Primary DI / UDI-DI
00842092170144 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Resilient dental precision attachment FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Preat by PREAT Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI 26a82bc2-aad8-4f25-9359-54e3d5ab820e 36 fields · synced May 31, 2026