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Perma-Hand

FDA UDI

Class II (US FDA UDI)

by Ethicon Inc.

Identity

Trade Name
PERMA-HAND FDA UDI
Generic Name
Silk suture FDA UDI
Device Name
Black Braided Silk, Nonabsorbable Surgical Suture FDA UDI
Model / Reference
N272H FDA UDI
Description
Black Braided Silk, Nonabsorbable Surgical Suture FDA UDI

Identifiers

Catalog Number
N272H FDA UDI
Primary DI / UDI-DI
10705031047372 FDA UDI
510(k) Number
K946173 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

No

FDA UDI

Category: Silk suture

A comprehensive overview of the PERMA-HAND medical device, including its features, compliance, and usage. This device is a type of non-absorbable surgical suture made from black braided silk.

Similar devices

Also classified as Silk suture.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ethicon Inc.

Sources (1)

  • FDA UDI d3b36608-623f-4763-9b4c-62fa362b497f 36 fields · synced Jun 22, 2026