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Hip Suture Passer — 35˚ Up

FDA UDIEUDAMED

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
Hip Suture Passer — 35˚ Up FDA UDI
Generic Name
Suturing unit, reusable FDA UDI
Model / Reference
D FDA UDI

Identifiers

Catalog Number
399431BSM FDA UDI
Primary DI / UDI-DI
10810190013523 FDA UDI
FDA Product Code
HWQ FDA UDI
GMDN Term
Suturing unit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing unit, reusable

Hip Suture Passer — 35˚ Up by T.a.g Medical Products Agricultural Cooperative Association — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Suturing unit, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI b6352ce2-88b0-4508-a08e-361340005c24 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026