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CurPro Silk Sutures Natural Material, Braided Black, Nonabsorbable

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
CurPro Silk Sutures Natural Material, Braided Black, Nonabsorbable FDA UDI
Generic Name
Silk suture FDA UDI
Device Name
3-0 EP 2, Length 18" , STERILE-EO FDA UDI
Model / Reference
9143 FDA UDI
Description
3-0 EP 2, Length 18" , STERILE-EO FDA UDI

Identifiers

Primary DI / UDI-DI
00616784914312 FDA UDI
FDA Product Code
GAP FDA UDI
GMDN Term
Silk suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5030 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: Silk suture

CurPro Silk Sutures Natural Material, Braided Black, Nonabsorbable by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silk suture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 55eaceca-bf98-4e06-8a79-20c25fc964ba 33 fields · synced May 30, 2026