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Knit-Pak

FDA UDI

Class U (US FDA UDI)

by Premier Dental Products Company

Identity

Trade Name
Knit-Pak FDA UDI
Generic Name
Gingival retraction cord, non-medicated FDA UDI
Device Name
Knit-Pak™ Knitted Retraction Size 2 FDA UDI
Model / Reference
9007555 FDA UDI
Description
Knit-Pak™ Knitted Retraction Size 2 FDA UDI

Identifiers

Primary DI / UDI-DI
00348783001907 FDA UDI
FDA Product Code
MVL FDA UDI
GMDN Term
Gingival retraction cord, non-medicated FDA UDI

Classification

Device Class
U 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

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

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: Gingival retraction cord, non-medicated

Knit-Pak by Premier Dental Products Company — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d28266f-4c86-49eb-9cbc-d73d7dfd755c 33 fields · synced Jun 8, 2026