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Mylar Foil - S/S RED - 7/8"

FDA UDI

Class I (US FDA UDI)

by Hager Worldwide, Inc.

Identity

Trade Name
Mylar Foil - S/S RED - 7/8" FDA UDI
Generic Name
Dental articulation paper FDA UDI
Device Name
Mylar Foil - S/S RED - 7/8" Articulating Paper FDA UDI
Model / Reference
72008 FDA UDI
Description
Mylar Foil - S/S RED - 7/8" Articulating Paper FDA UDI

Identifiers

Primary DI / UDI-DI
D248720080 FDA UDI
FDA Product Code
EKF FDA UDI
EFH FDA UDI
GMDN Term
Dental articulation paper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
872.6140 FDA UDI
Commercial Distribution
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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental articulation paper

Mylar Foil - S/S RED - 7/8" by Hager Worldwide, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental articulation paper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3fca8797-7958-45e5-9366-f49929cd4f1d 34 fields · synced Jun 9, 2026