← Back to catalogue

Supramid Extra

FDA UDI

Class II (US FDA UDI)

by S. Jackson, Inc.

Identity

Trade Name
SUPRAMID EXTRA FDA UDI
Generic Name
Nylon suture, non-bioabsorbable, multifilament FDA UDI
Device Name
1/2 Circle Taper Point Needle (18.7mm), USP 4-0 SUPRAMID EXTRA white cable-type Nylon, 40" Loop FDA UDI
Model / Reference
Code RJH-40-40 FDA UDI
Description
1/2 Circle Taper Point Needle (18.7mm), USP 4-0 SUPRAMID EXTRA white cable-type Nylon, 40" Loop FDA UDI

Identifiers

Catalog Number
Code RJH-40-40 FDA UDI
Primary DI / UDI-DI
00816848024005 FDA UDI
FDA Product Code
GAR FDA UDI
GMDN Term
Nylon suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5020 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

No

FDA UDI

Category: Nylon suture, non-bioabsorbable, multifilament

Supramid Extra by S. Jackson, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nylon suture, non-bioabsorbable, multifilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
S. Jackson, Inc.

Sources (1)

  • FDA UDI cc15a636-c151-4cfd-88e3-234394ef1930 35 fields · synced May 30, 2026