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Quill

FDA UDI

Class II (US FDA UDI)

by Surgical Specialties México, S. de R.L. de C.V.

Identity

Trade Name
Quill FDA UDI
Generic Name
Barbed polyester suture, non-antimicrobial FDA UDI
Device Name
Quill PDO 2-0 Violet 45cm RB-1 Uni FDA UDI
Model / Reference
VLP-4222 FDA UDI
Description
Quill PDO 2-0 Violet 45cm RB-1 Uni FDA UDI

Identifiers

Primary DI / UDI-DI
00848782051625 FDA UDI
510(k) Number
K132268 FDA UDI
FDA Product Code
NEW FDA UDI
GMDN Term
Barbed polyester suture, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4840 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Barbed polyester suture, non-antimicrobial

Quill by Surgical Specialties México, S. de R.L. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Barbed polyester suture, non-antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45088fc4-e4f8-4e50-a9a1-9aaafeb67dbe 34 fields · synced May 30, 2026