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Bioviva-3D Dental

FDA UDI

Class II (US FDA UDI)

by 3d Dental Designs And Development, Llc

Identity

Trade Name
Bioviva-3D Dental FDA UDI
Generic Name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
Device Name
Basik PGC SUTURE USP 2/0..3/8 REV CUTTING NEEDLE 30MM LENGTH One Device FDA UDI
Model / Reference
BPCG943 FDA UDI
Description
Basik PGC SUTURE USP 2/0..3/8 REV CUTTING NEEDLE 30MM LENGTH One Device FDA UDI

Identifiers

Primary DI / UDI-DI
00817169021124 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Category: Polyester suture, bioabsorbable, monofilament, non-antimicrobial

Bioviva-3D Dental by 3d Dental Designs And Development, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, bioabsorbable, monofilament, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3d Dental Designs And Development, Llc

Sources (1)

  • FDA UDI 158360df-17b7-4c63-908e-1e6f42faf8ec 33 fields · synced May 30, 2026